Basic Properties of Neural cells

Mature nerve cells are unable to divide and with very few exceptions cannot regenerate their

cell processes. In humans 10-100 billion cells are provided at birth, the natural daily loss of

about 10,000 cells throughout life causing only a negligible reduction of the entire cell

population. Considering that each cell makes about 1,000 synaptic contacts (resulting in 10-

100 thousand billion total contacts) the enormous complexity of neuronal wiring in the human

brain becomes apparent.

Basically, nerve cells consist of a cell body (soma or pericaryon) from which two

functionally different types of cell processes emanate: dendrites are often highly branched and

receive electrical signals from other neurons. In some cases, their surfaces are covered with

small protrusions called dendritic spines. Axons (also called neurites) send out electrical

signals. In contrast with dendrites, they are of uniform diameter along their entire length, which

can vary considerably. Axons can be divided into one or several collaterals forming right

angles with the main axon. Their tips are often highly branched, leading to the formation of up

to 1,000 nerve endings per axon. Synapses are specialized structures at nerve endings allowing

chemical or electrical signal transfer to target cells (for details see below).

Besides neurons the population of brain cells additionally comprises glial cells most of

which are able to divide throughout life. In contrast with neurons glial cells typically possess a

uniform set of cell processes and usually are significantly smaller than neurons. Four major

subtypes of glial cells are known (astrocytes, oligodendrocytes, microglia, Schwann cells) each

having its own specialized cellular functions (for details see chapter “Properties of Glial

Cells” on page 17). There is a close physiological dependence and functional cooperation

between neurons and glial cells in the nervous system.

The structural (morphological) analysis of neural cells (i.e., neurons and glia) is greatly

hampered by the enormous number and structural complexity of these cells in the brain tissue.

Staining of thin tissue sections with non-specific dyes (8 μm thickness, 1000 μm = 1 mm) is

frequently used for microscopic analysis of brain tissue. By this technique, however, most of

the cell processes are not visible due to low contrast of these fine structures and are also cut off

and hence cannot be traced over longer distances.

However, at the end of the nineteenth century a technique was devised by Camillo Golgi and

Ramon y Cajal that allows to completely stain a small subset of the neural cell population with

silver salts (silver impregnation). This allowed to discriminate a large number of neuronal cell

types mainly on the basis of their dendritic tree shape. Although the neuronal morphologies areassessed by novel, computer-based approaches for a more precise classification, there are

classically four basic categories described.

  • Multipolar neurons – the most predominant in the brain and spinal cord and are inclusive

of motor neurons as well as interneurons. These cell types have a single axon extending

from one end of the cell body and several dendrites branching as they protrude from the

other side of the cell body.

  • Bipolar neurons – that are only associated with afferent impulses. They have a single axon

projecting from one end of the oval cell body and a lone dendritic tree extending from the

other end.

  • Unipolar neurons – have a single axon projecting from the spherical cell body.

  • Pseudounipolar neurons – have one single process bifurcating close to the cell body that

serves both the role of the axon and the role of the dendrite.

Shapes of dendritic trees are highly variable from one neuronal type to another within each

class, and this diversity contributes to differential processing and computation of synaptic or

sensory inputs. Dendritic geometry plays key roles in shaping intrinsic firing patterns, and

coincidence detection.Intracellular structures

The cell is filled with cytoplasm, which is a thick, gelatinous solution that is enclosed by the

cell membrane. It is mainly composed of water, salts, and proteins and provides an environment

for many cellular processes to occur, such as protein synthesis, the first stage of cellular

respiration (known as glycolysis), etc. The cytoplasm of neural cells contains a highly efficient

scaffolding system that is required to stabilize the extensively branched cellular structure and

to concomitantly allow for structural flexibility and material transport. This so-called

cytoskeleton comprises three major classes of protein fibers of different sizes, structures and

chemical composition:

Microtubules are long unbranched hollow tubes of approx. 20 nm diameter

(1 Mio nanometers = 1mm), that consist of the protein tubulin as dimers that are in

building mainly 13 protofilaments arranged in a hollow tube.

Neurofilaments are long solid filaments of 10 nm diameter, that consist of three neuron-

specific neurofilament proteins. They have flexible polymer arms standing out that

repel neighbouring neurofilaments. The neurofilaments determine the radius of the

axon. Glial cells possess glial filaments instead consisting of the glial fibrillary acidic

protein (GFAP).

Mikrofilaments or actin-filaments are small solid filaments of 5 nm diameter,

consisting of the globular monomeric protein actin. They are even more abundant in

muscle cells, where they support muscle contraction.

All three cytoskeletal elements are organized into networks that resist deformation but can

reorganize in response to externally applied forces or internal stimuli.

In addition, neural cells contain a number cell organelles that are fundamental for cell

survival in general and hence occur in any other cell type as well *****

.

• In the nucleus the complete genetic material of an organism is stored in the form of

deoxyribonucleic acid (DNA). Since in a given cell only a limited set of genes is

converted into proteins highly specific control mechanism of gene activation are

needed which operate in a cell type and cell stage-specific manner. The process of

gene activation is initiated by gene transcription (biosynthesis of messenger RNA),

being regulated by proteins called transcription factors.

• In the endoplasmic reticulum (ER) protein and lipid biosynthesis are taking place.

Protein biosynthesis (translation) requires the presence of ribosomes on the ER

surface which associate there with mRNA produced in the nucleus.• In the Golgi-complex proteins are sorted and packaged into transport vesicles.

Dependent on their individual content some of these vesicles fuse with the plasma

membrane, while others deliver their content to predestined intracellular sites.

• In the mitochondria the energy required for cell survival is generated in a storable form.

The complex physiological mechanisms underlying energy production and storage

include the biochemical breakdown of glucose ultimately leading to the production

of adenosine-tri-phosphate (ATP), the main energy storage molecule of all cells.

This process works efficiently only in the presence of oxygen. Nerve cells

permanently have high energy consumption and hence are heavily dependent on a

constant glucose and oxygen supply via the blood stream.

_________________________________

  • Neural cells share many basic properties with other cells**.** For a more detailed description of these

basic cell biological features and functions the reader is referred to classical cell biological textbooks.Axonal transport

Intracellular transport of material between the cell body and the cell processes is of vital importance

for nerve cells. This is particularly obvious in the case of nerve endings which are often quite

remote from the soma, where nearly all of the biosynthetic processes are taking place. Regarding

the velocity and type of material being translocated two major classes of axonal transport can be

discerned:

• The slow axonal transport shows a velocity range of 1- 6 mm per day. It transports proteins

of the cytoskeleton (see above) and supports nerve fiber growth during development and

regeneration.

• The fast axonal transport has a velocity range of 100-400mm per day. It transports larger

particles such as vesicles or even mitochondria. Besides an anterograde transport from

the cell body to the nerve ending a retrograde transport running in the opposite direction

occurs. Fast axonal transport is guided by microtubules and is carried by specialized

vehicle proteins that bring their cargo to the desired site. Anterograde transport is effected

by the protein kinesin, while retrograde transport relies on the protein dynein. Both are

called motor-proteins which use ATP as energy source for transport activity.

The molecular mechanism underlying kinesin driven axonal transport has been analyzed in great

detail. It provides a striking example of how proteins can do work in the presence of ATP. From

the structure of the kinesin molecule valuable evidence about its mode of operation could be

deduced. It consists of two very similar subunits (“dimer” structure), each containing a globular

motor domain for binding and processing of ATP as well as a rod-like stalk domain that fixes the

cargo to the vehicle. Both are linked by a flexible hinge region.

Transport activity is initiated by the splitting of an ATP molecule that is bound to one of the motor

domains. This leads to a structural reorganization of the kinesin protein that lifts off one of his

motor domains from the microtubule surface and moves it forward to become fixed on the

microtubule surface again (hand-over hand walking model).

The consumption of one molecule of ATP is sufficient for an eight nm step of a single kinesin

molecule on the surface of a microtubule towards the nerve ending.

As will be outlined later controlled changes of a proteins 3-D structure is a fundamental

mechanism to regulate its functional activity.Basic Properties of the Neuronal Plasma Membrane

The entire neuron, like all other cells, is enclosed by a plasma membrane – a double layer mainly

composed of phospholipid molecules (for details see below) - acting as a barrier preventing the

contents of the cell from mixing with those of the extracellular space. The plasma membranes of

most cells consist by half of proteins and by half of lipids. Phospholipids, which form the major

part of membrane lipids, are rather complex molecules consisting of two highly hydrophobic fatty

acid chains, that are linked via glycerol to the hydrophilic head groups of the molecule. The latter

include a phosphate group which depending on the subtype of phospholipid carries another

characteristic hydrophilic constituent: e.g., choline in the case of the phospholipid lecithin. In total,

phospholipids possess a hydrophilic portion (headgroups) and a hydrophobic portion (fatty acid

tails). From this mixed hydrophilic-hydrophobic property the behaviour of phospholipids in the

aqueous environment of a cell can be predicted: when dropped on a water surface, phospholipid

molecules will evenly spread out in a single molecular layer with the headgroups contacting the

water surface and the fatty acid tails oriented to the opposite side. In the plasma membrane, actually,

two layers of phospholipid molecules are joined together. The fatty acid groups of each layer are

facing each other in the hydrophobic center of the membrane, while the headgroups are aligned on

either side of the membrane surface. The core of the plasma membrane thus forms an efficient

barrier against the passage of hydrophilic molecules.

The second major constituents of the neuronal plasma membrane, the proteins, are much

more complex in their biochemical composition, their structure and their functions. The building

blocks of proteins are amino acids. They all share two basic structural elements: an amino group

and an acidic group, while the rest of the molecule is highly variable. Hence these residual groups

alone determine the physico-chemical properties of an amino acid. Some of them are hydrophobic

others are hydrophilic. Some are acidic, while others are basic. As a whole twenty different species

of amino acids are sufficient to create the huge number of different protein molecules that occur in

a living organism.

Since proteins are chains of amino acids of variable length and composition their

fundamental properties are defined by their amino acid sequence (primary structure of the

protein). Under normal physiological conditions a protein will, however, not exist as a long

unfolded chain of amino acids (polypeptide chain) but will adopt higher order structures that are

more or less determined by the individual amino acid sequence. Two types of highly regular

secondary structures can be observed:

• An alpha helix is generated when a single polypeptide chain turns regularly about

itself to make a rigid cylinder.• A beta sheet is formed when an extended polypeptide chain folds back and forth upon

itself, with each section of the chain running in the direction opposite to that of its

neighbours. This gives a very rigid structure.

• Besides a rather irregular random coil structure is quite frequently found as well. This

often forms the more flexible parts of a protein.

In most proteins all three structural elements coexist in the various regions at different proportions

resulting in highly characteristic folding patterns.

The next level of structural organization of a protein is called tertiary structure or conformation

giving the protein its characteristic overall three-dimensional shape. It is stabilized by chemical

bonds between the variable residues of amino acids. As described above for the motor protein

kinesin targeted changes in the 3D-shape of a protein (also termed conformational changes)

typically coincide with the onset and offset of specific functional activities of a protein. In some

proteins, such as kinesin, several polypeptides (so-called subunits) are grouped together to form a

functional unit. Kinesin, containing two subunits is called a “_di_mer”. Proteins consisting of four

subunits would be called “_tetra_mers”.Structural characterization of proteins

For the structural analysis of proteins, a wide range of biochemical and biophysical techniques are

available. The primary structure is obtained by biochemical methods, either by direct

determination of the amino acid sequence from the isolated protein or indirectly - but much more

rapidly, from the nucleotide sequence of the corresponding gene or cDNA. To obtain the

secondary structure CD-spectroscopy is the method of choice. In many cases the secondary

structures of a protein can be predicted from its amino acid sequence by computer. For the

determination of the tertiary structure or conformation a combination of very time-consuming

and highly demanding biochemical and biophysical techniques are required: initially the protein of

interest must be isolated in high purity and relatively large amounts (several milligrams) to allow

its crystallization. Unfortunately, this is a poorly predictable process, which is not always

successful even in the hands of experts. Subsequently the three-dimensional structure can be

solved by x-ray crystallography.

Most powerful x-ray beams are generated in synchrotron storage rings where electrons travel

close to the speed of light. The parallel beams of x-rays are diffracted by the protein crystal and

the characteristic diffraction pattern is recorded on a detector or x-ray film. From this the atomic

structure of a protein can be calculated.

Functions and Features of Enzymes

Enzymes are a special class of proteins which are important for the control of virtually all vital cell

functions. As should be expected they comprise an enormously large number of protein families

that control a huge diversity of biochemical reactions in a cell. The molecule which is

biochemically modified by a given enzyme is called its substrate. The name of an enzyme is

determined by adding the ending -ase to the name of its substrate: an enzyme modifying DNA

would be called DNAse, one that modifies ATP would be called ATPase. The specificity of an

enzyme for its substrate is due to mutual structural matching similar as a key match to its lock. The

activity of an enzyme hence can be efficiently controlled by slightly modifying its tertiary structure

to induce matching or mismatching of the binding pocket with its substrate, respectively. Many

enzymes split their substrate into fragments of various sizes and/or numbers. Digestive enzymes

are well known examples. Enzymes that split ATP into ADP and phosphate (ATPases) are

particularly important for cells, since they allow the release of stored energy to be used for all sorts

of physiological processes (see for example the paragraph about the sodium-potassium pump).

Another class of enzymes controls the activity of other proteins (including other enzymes!), instead.

They do this by attaching to or removing phosphate residues from their substrate, which induces a

conformational change in the substrate protein. Such enzymes are collectively called –kinases. If

their substrate is a protein, they are called protein kinases.Membrane Proteins

Membrane proteins are particularly important in nerve cells, since they control physiological

interactions and signalling with other cells. Since proteins are highly hydrophilic molecules the

question arises how their association with the hydrophobic parts of phospholipid membranes can

be accomplished. While it is easily understood that proteins can be fixed on either membrane

surface as so-called peripheral membrane proteins the question remains how proteins can

become deeply embedded into the hydrophobic core as so-called integral membrane proteins.

As mentioned above, the building blocks of proteins, the amino acids widely differ in their side

chain properties. Among the twenty amino acids used for protein biosynthesis several possess

highly hydrophobic side chains. This allows to inserting such stretches of a polypeptide chain into

the core of a membrane that are composed of hydrophobic amino acids. By computer-assisted

screening of the amino acid sequence of protein stretches comprising at least 20 hydrophobic

residues in series can be identified and related to membrane-spanning segments of a protein

(transmembrane segments). Some proteins contain only a single transmembrane segment, while

others exhibit more then 10. In several cases the number of these segments is useful to classify

protein families.

Bioelectricity

Electricity generally requires the separation of charges to take its rise. Technical electricity is based

on the movement of electrons and hence works extremely fast. In living cells electrical signalling

involves the movement of ions, instead, including both negative (i.e., anions such as chloride) as

well as positive charges (i.e., cations such as sodium, potassium, or calcium ions). Since ions are

enveloped by water molecules, they are highly hydrophilic and hence cannot easily pass the lipid

bilayer of a plasma membrane. Membrane potentials are built up by an unequal distribution of

charges on both sides of a membrane. The neuronal plasma membrane collects charges on either

surface similar like a capacitator. Due to its large surface area and small thickness, it possesses a

relatively high capacitance (C= area/distance).

During the pioneering days of electrophysiology, the squid has proven as a valuable animal

model: due to its relatively large size (> 0.5 mm in diameter) the squid giant axon allowed to record

membrane potentials with rather coarse technical equipment. Most of the basic information about

electrical signalling in nerve cells was gained by experiments performed on this system in the

middle of the 20th century by Alan Hodgkin and Andrew Huxley.

The ionic composition of the squid axonal cytoplasm (intracellular compartment) in fact greatly

differs from those of the extracellular body fluids (blood or sea water): while the sodium ion

concentration (Na**+**

) is approx. eight-fold higher in the extracellular fluid than in the axoplasm thereverse is true for potassium (K****+

), which occurs in an about twenty-fold higher concentration in

the axoplasm as compared to the extracellular space. Chloride is enriched in the extracellular fluid,

similar as sodium. To maintain such steep gradients of ionic concentrations active transport

mechanisms are necessary. The unequal distribution of sodium and potassium is accomplished by

a so-called sodium-potassium pump which is fuelled by ATP (about two thirds of the total energy

consumption of a nerve cell is due to this process!). This pump is a large membrane protein with

ten transmembrane segments. The intracellular portion harbours an ATP-binding site. This site is

able to split ATP enzymatically into ADP and phosphate, hence it acts as an ATPase.

In total the transport process is an unequal exchange of sodium for potassium ions: for

three sodium ions transported out of the cell two potassium ions are carried in. The molecular

mechanism underlying this ion exchange process has been -and still is being- analysed in great

detail. The splitting of bound ATP leads to a conformational change in the intracellular part of

the sodium-potassium pump so that sodium becomes occluded in a binding pocket close to the

membrane. Subsequent removal of ADP opens the binding pocket and releases sodium into a

hydrophilic tunnel between the transmembrane segments of the pump protein. Ensuing removal of

the phosphate residue that was split of from ATP evokes another conformational change which

now occludes potassium ions in a binding pocket at the extracellular face. Binding of a new ATP

causes potassium release into the cytoplasm. The process is constantly repeated as long as enough

ATP is available. The unbalanced exchange of sodium for potassium makes (3:2) makes only a

small contribution to the membrane potential. The major part comes from a selective permeability

of the membrane for potassium ions but not for sodium (see below).

The Resting Membrane Potential

Since the plasma membrane is selectively leaky to potassium ions, potassium diffuses out of the

cell, following the concentration gradient previously built up by the sodium-potassium pump. The

efflux of these cations creates a significant electrical potential across the membrane that finally

prevents further outward diffusion of potassium. When both forces (chemical ion gradient and the

counteracting electrical potential) are at equilibrium a stable membrane potential is attained,

which is called resting potential. The resting potential seems to be mainly determined by the

outward diffusion of potassium ions. This hypothesis can be tested by a mathematical approach.

The Nernst Equation

The Nernst equation allows for calculating electrical potentials (E

x

) that are generated by the

diffusion of ions.E

x

= RT/_z_F ln [X

+

]

o

/[X

+

**]**i

where R is the gas constant, T the absolute temperature in degrees Kelvin, z is the charge of the

ion, and F is the Faraday constant, while [X

+

]

o

is the extracellular and [X

+

**]**i

the intracellular

concentration of ion X. For monovalent ions (such as sodium or potassium) at room temperature

the equation reduces to

E

x

= 58 mV log****10 [X

+

]

o

/[X

+

**]**i

Insertion of the extracellular and intracellular potassium ion concentrations as measured for the

squid giant axons leads to

E

x

= 58 mV log****10 (20/400)

E

x

= 58 (-1.3) mV = -75 mV

This value is quite close to the resting potential determined experimentally for the squid giant axon

albeit being slightly less negative (-70 mV). Accordingly, the resting potential in fact is mainly due

to the diffusion of potassium ions, but not exclusively. Other ions, including sodium and chloride

make a certain contribution, too. To consider these ions properly the Nernst equation was extended

by Goldman, Hodgkin and Katz as follows:

where p is the permeability factor for a given ion.

E

x

= RT/zF ln

p Na [Na+

]i + p K [K+

]i + p Cl [Cl

]

o


p Na [Na+

]

o

  • p K [K+

]

o

  • p Cl [Cl

]iThe Action Potential

Experimental manipulation of the resting potential in principle can be done in two ways: injecting

current by a microelectrode will further increase the potential difference across the membrane,

leading to hyperpolarization of the membrane. If the polarity of the microlectrode is reversed

before current injection this will lead to a decrease in the potential difference, an effect called

depolarization. If a short current pulse is applied that leads to only a small depolarization the

membrane potential will passively follow and thereafter rapidly return to the resting potential again.

The situation is very different, however, with larger depolarizing stimuli. At around -40 mV

depolarization a critical strength, or threshold, is reached. Beyond this threshold, one observes a

strongly overshooting depolarization that is superimposed on the passive response and lass for

several milliseconds. Typically, the depolarization goes beyond 0 mV leading to a change in

polarity, i.e., the inside of the neuronal membrane becomes briefly positive relative to the

extracellular side. This active response is called action potential. An important property of action

potentials is that they are all-or-none events: if the stimulus strength is further increased the action

potential will retain its size. As a consequence, information about stimulus intensity must be

encoded by a different mechanism. If a given stimulus is lasting longer a whole series of action

potentials will be evoked. With increasing stimulus intensity, the delay between consecutive action

potentials decreases as a whole leading to a higher frequency of action potentials (frequency code).

Refractory period

If pairs of stimuli are applied to a nerve at varying temporal intervals the minimal interval required

to achieve a normal response can be determined. These experiments show that for several

milliseconds after firing an action potential, it is impossible to evoke another action potential, no

matter how large the depolarizing stimulus is. In other words, the axon is refractory to stimulation

during this period. This absolute refractory period is followed by a relative refractory period

during which the second action potential is of smaller size than the first one. In subsequent chapters

it will be shown that the refractory period is important to maintain unidirectional signal

propagation along a nerve fiber. Furthermore, the molecular basis of electrical unresponsiveness

will be addressed.Ionic mechanisms underlying the generation of action potentials

The sodium hypothesis

A most obvious explanation for the fast membrane depolarization that coincides with an action

potential would be a sudden change in the permeability of the neuronal plasma membrane for

sodium, leading to a sodium influx according to the sodium concentration gradient. To prove this

hypothesis the extracellular sodium concentration was lowered experimentally. Under these

conditions action potentials started with a considerable delay and were of smaller size. By gradually

lowering the extracellular sodium concentration this effect became more and more pronounced.

The voltage clamp technique

In order to directly measure the ionic currents underlying an action potential a novel technique was

applied, termed voltage clamp technique. It consists of an electronic feedback system that holds

the membrane potential constant at a voltage chosen by the investigator. In its simplest form the

voltage clamp consists of two separate electrodes, one connected to a voltage and the other

connected to a current-passing amplifier. A negative feedback loop is created by adding a

feedback amplifier, which compares the voltage set by the experimenter (so-called command

voltage) with the measured membrane voltage. As mentioned above during an action potential the

membrane voltage normally changes in a depolarizing direction. During a patch clamp experiment

this change in membrane voltage is carefully compensated by current injection via the current-

passing amplifier under the control of the feedback amplifier. The size of the compensating current

is equal to those of the ionic current that flows through the cellular membrane during an action

potential.

Ionic currents underlying an action potential

By such an approach Hodgkin and Huxley were able to record membrane currents of the squid

giant axon that occurred after setting the membrane potential to 10mV, being well above the

threshold for an action potential. They found a biphasic current response consisting of an early

inward current that after a few milliseconds was superimposed by a delayed outward current.

By ionic substitution experiments they could show that the early inward current was carried by

sodium ions, while the remaining outward current was carried by potassium ions. As a whole the

characteristic of the sodium current fitted very well with the membrane depolarization occurring

during the rising phase of an action potential while thepotassium current suited best with the ensuing membrane repolarization. A most remarkable

property of the sodium current was its spontaneous inactivation a few milliseconds after its initial

rise.

Pharmacology of ionic currents

In order to better characterize the protein pores through which sodium and potassium ions flow

during an action potential a selective blockade of either current was desired. The poison of the

buffer fish (Tetrodotoxin, TTX) proved as a very useful pharmacological tool for this purpose. It

precisely fits into the opening of the sodium channel protein, but is too large to penetrate the pore.

By plugging the pore TTX selectively prevents sodium influx into the cell. As a consequence,

action potentials are no longer generated ultimately leading to the death of the animal that has taken

up the poison. For the experimenter the application of TTX allows to study the potassium current

in isolation, since potassium ions flow through separate channels, that are not affected by TTX.

A selective blockade of potassium channels is possible by application of the small organic molecule

tetra-ethyl-ammonium (TEA), which allows to recording sodium currents in isolation. By these

experiments it was proven that at least two different types of protein channels occur in the

neuronal plasma membrane one selectively permeable for sodium the other for potassium.

Isolation and functional characterization of the sodium channel protein

Channel-specific toxins such as TTX were also of great help for the biochemical isolation and

purification of the sodium channel protein. The electric organ of the electric eel proved as most

suitable starting material, since it was relatively enriched of voltage-gated sodium channels. With

the aid of radioactively-labeled toxin a high molecular weight protein could be identified that made

up the pore-forming complex (α-subunit) of the voltage-gated sodium channel which was

accompanied by two accessory β**-subunits** of much lower molecular size. With the purified

channel protein available it became possible to clone and sequence the cDNA encoding the protein

by methods of gene technology. The amino acid sequence of the α-subunit was deduced from the

nucleotide sequence of its cDNA and subsequently screened for transmembrane segments (see

chapter “Membrane Proteins”). It turned out that the channel protein possessed four large

domains of similar structure, each including six transmembrane segments (S1-S6). One of these

(S4-segment) appeared quite unusual, since it contained several positively charged amino acid

residues. Furthermore, the region connecting S5 and S6 revealed a hairpin loop structure.In order to verify the electrophysiological properties of the isolated channel protein and to compare

it with those of native sodium channels the cDNA was converted into mRNA by in vitro-

transcription. The resulting mRNA was injected into unfertilized eggs (“oocytes”) of frogs. The

frog oocytes “accepted” the foreign mRNA and produced large amounts of sodium channel protein.

By subsequent electrophysiological recoding the voltage-gated sodium current of the frog oocytes

could be compared with those occurring naturally in neuronal cells. This technique additionally

allowed to performing all sorts of genetic manipulations of the sodium channel cDNA before

expressing it in frog oocytes. By this approach the specific functional roles of several of parts of

the channel protein could be experimentally elucidated. First of all exchanging the positively

charged amino acids of the S4 segments for neutral ones abolished the voltage-sensitivity of the

channel protein, emphasizing that S4 represents the voltage-sensor of the channel. Secondly it

was shown that the intracellular loop connecting the third and the fourth domain of the channel

protein is responsible for the spontaneous channel inactivation. Thirdly the four hairpin loops

connecting the S5 and S6 segments together build the wall of the hydrophilic channel pore.

In the case of potassium channels the lack of a rich source of channel protein made a different

approach necessary. In the fruit fly Drosophila a mutation was identified that showed an

unexpected behaviour under ether anaesthesia. Unlike normal flies this mutant, called Shaker,

shook its legs and wings, suggesting some neurological deficit. Electro-physiological recording

revealed a prolonged duration of action potentials, as would be expected if the potassium channel

conductance was reduced. Voltage-clamp studies in fact revealed a strong reduction of the

potassium outward current. Molecular biological analysis of the mutated gene locus (making use

of a technique called “positional cloning”) allowed to isolating and sequencing the underlying gene.

The deduced amino acid sequence of the encoded potassium channel showed remarkable

similarities with those of the sodium channel. It included, however, only a single large domain

comprising six transmembrane segments (to form a functional potassium channel, however, four

of these subunits are grouped together). As described above for the sodium channel the S4-

segment was rich in positively charged amino acids and there was a hairpin loop between S5 and

S6. As a whole, both channel classes were obviously sharing basic structural elements. More close

inspection of the Shaker locus revealed the presence of several other potassium channel genes,

encoding various families of potassium channels with different electrophysiological properties.

Corresponding genes were later identified in mouse and human as well.Single channel analysis

By the invention of the patch clamp technique (developed by Erwin Neher and Bert Sakmann) it

became possible to directly measure the activity of single ion channels (“single channel

recording”). In contrast with traditional methods using sharp microelectrodes to penetrate the cell

membrane, the surface of a patch clamp glass electrode (patch pipette) is quite smooth. The patch

pipette is gently placed against the cell surface (attached patch). Subsequent patch clamp recording

can be done in one of three different configurations. In the first case (whole-cell mode) the

experimenter applies suction through the pipette to disrupt the membrane patch under the electrode,

thus fusing the cellular cytoplasm with the fluid in the patch pipette. By this technique the activity

of all ion channels in the plasma membrane of a cell is collectively measured. To obtain single

channel recording the patch pipette is retracted from the cell surface thus pulling apart a small

piece of membrane that ideally contains only a single ion channel (inside-out and right side-out

configuration, respectively). Under these conditions typical current fluctuations become visible

reflecting the opening and closing of an individual ion channel. In the case of voltage-gated

channels the open-probability increases with the degree of membrane depolarization. By applying

various command voltages and plotting the current against the applied voltage the single channel

conductance of an ion channel can be determined (measured in Pico-Siemens, 1 pS =

1pAmpere/1Volt).Axonal Signal Propagation

An action potential is not a local event but it moves along an axon to finally reach its nerve ending.

What are the mechanisms driving it away from its initial site of generation? Since a quite similar

task is performed by electrical cables in technical systems the question arises if axons might work

in a comparable manner.

Cable properties of an axon

The passive properties of an axon (so called cable properties) can only be studied if the active

physiological mechanisms are experimentally suppressed. This can be most easily achieved by

local cooling of a nerve fiber. Under these conditions a local depolarization applied to a nerve

fiber still passively spreads to both sides (electronical spread). Similar as in electrical cables the

spread of electrotonical potentials along an axon is dependent on the resistance and the

capacitance of the fiber. Due to the relatively high internal resistance of axons, the electrotonic

potential, however, is decaying exponentially so that it will move only a few millimetres away

from its original site. This distance is determined by the size of the fiber. Larger fibers that have a

lower resistance allow for a wider spread of the potential.

Active signal propagation

What are the active mechanisms that amplify the signal allowing it to travel over longer distances?

Under normal physiological conditions voltage-gated sodium channels residing in the membrane

regions ahead of a depolarized site will become activated if a certain threshold of depolarization is

achieved. They will then produce a full-size action potential at the novel site (obeying the all or

none law). Sodium channels residing in membrane areas behind the site of original stimulation

normally are still inactivated (refractory period!), hence the signal is conducted only in one

direction. By constantly repeating passive electrotonical spread and re-amplification via sodium

channel activation, the signal continuously travels along the axon, without any loss of signal

strength.

By this mechanism of continuous impulse conduction maximal velocities of up to

25m/sec can be achieved. A well-known example is the squid giant axon, which has a diameter of

more than half a mm. Since the conduction velocity increases only with the square root of the

fiber diameter, increasing the fiber size at a certain point becomes inefficient and costs a lot of

space in the nervous tissue.Myelination

An alternative mechanism, which occurs in vertebrate species only (comprising fish, amphibia,

reptiles, birds, and mammals), is provided by surrounding the nerve fiber with an insulating sheath

(so called myelin sheath). This sheath is periodically interrupted at the nodes of Ranvier. Only at

these sites action potentials can be generated, since voltage-gated sodium channels are heavily

clustered there. Hence in a myelinated nerve fiber the signal does not move continuously along the

axon membrane but jumps from one node to the next (saltatory impulse conduction). This type

of signal propagation is not only faster but also less energy consuming than the continuous mode

of conduction, since energy consuming ion transport (sodium-potassium ATPase) is limited to the

nodes of Ranvier. The insulating sheath of myelin enhances impulse conduction by two basic

mechanisms:

• the leakage current across the axonal membrane is reduced

• the membrane capacitance is decreased

Taken together both factors allow for a faster and wider spread of electrotonic potentials until the

next node of Ranvier. In myelinated nerve fibers there is a linear relationship between axon

diameter and conduction velocity. The myelin sheath is not a product of the neuron itself but is

generated by two highly specialized populations of glial cells. In the peripheral nerve fibers myelin

is generated by Schwann cells, while in the central nervous system (CNS: brain and spinal cord)

this task is performed by oligodendrocytes. While a Schwann cell produces only a single myelin

segment, each of the oligodendrocytes sends out several cell processes to form a multitude of

myelin segments on different nerve fibers. In both cases myelin represents a modified plasma

membrane of the glial cell being wrapped around the axon in many turns. By squeezing out the

cytoplasm between the overlapping membranes a compact multilayered membrane sheath is

formed. This structure is strongly stabilized by a set of myelin-specific adhesion proteins.

Myelin proteins

Membrane apposition at the cytoplasmic side is accomplished by a set of fairly low molecular

weight basic proteins (MBP) that associate at the intracellular membrane surfaces.

Furthermore, a highly hydrophic proteolipid protein (PLP) with four transmembrane segments is

involved in the extracellular membrane apposition. While MBP is common to both Schwann cells

and oligodendrocytes PLP is unique to myelin and myelin-forming cells of the CNS. In the myelin

of peripheral nerve fibers PLP is replaced by the P0-glycoprotein.P

0 possesses a single transmembrane segment. Its extracellular domain has an antiparallel β-sheet

structure as is typical for many cell adhesion molecules, in general. P0 provides for a stable contact

at the extracellular membrane faces.

Multiple sclerosis

Multiple sclerosis is the most frequent demyelination disease in the Western world. It is an

autoimmune disease caused by auto-antibodies against myelin-specific proteins, in particular

against myelin basic protein (MBP). According to the molecular mimicry theory it is assumed

that certain viruses (in particular the measle virus) can carry proteins that share structural

similarities with MBP into an infected organism, which subsequently produces antibodies against

these protein structures. Due to the blood-brain barrier these antibodies normally do not have access

to MBP in the brain. However, once a local and transient break of the barrier occurs, myelin in

the vicinity of the afflicted blood vessels become destroyed by immune cells from the blood stream.

Properties and Functions of Glial Cells

Apart from oligodendrocytes and Schwann cells which are responsible for myelination in the

central and peripheral nervous system, respectively, two additional types of glial cells occur in the

CNS (brain and spinal cord).

Astrocytes

Astrocytes have many cell processes that radiate out from the cell body in all directions, giving

them a star-like appearance, and possess a cell-type specific cytoskeleton protein, the glial

fibrillary acidic protein (GFAP). Their cell branches are in close contact with blood vessels on

the one side and with nerve cells on the other. Hence, they provide nutrients coming from the

blood stream (e.g. glucose) to nerve cells and they perform metabolic waste removal. A most vital

function is the removal of certain neurotransmitters (such as glutamate and GABA, see below)

from the extracellular space, which may become harmful to nerve cells if they stay there for a too

long time. Furthermore, astrocytes balance out the extracellular potassium concentration thus

regulating the excitability of nerve cells. More recently a participation in neuronal signal

processing has been reported.

Microglia

Microglial cells are small ramified cells that occur throughout the adult central nervous system.

Following injury, they become activated and start to divide and migrate to the site ofinjury and probably transform there into macrophage-like cells, being capable of clearing damaged

cells and debris by phagocytosis. In similarity with lymphocytes activated microglia express a

variety of immunomodulator peptides and surface receptors involved in immune defence.

Neurotransmission

The neuromuscular junction is a specialized type of synapse, connecting the nerve ending of a

motor nerve with a skeletal muscle fiber. Due to its relatively large size and convenient

experimental access, it has served as a model system to analyze the basic factors and mechanisms

underlying chemo-electrical signal transfer from a nerve terminal to a target cell

(neurotransmission). The pioneering experiments done by Sir Bernard Katz revealed that shortly

after the arrival of an action potential at the nerve ending a small potential is generated in the

neuromuscular junction that triggers the formation of a muscle action potential. It is called endplate

potential and it can be efficiently blocked by the poison curare. By carefully titrating the amount

of curare applied to the neuromuscular junction the endplate potential can be recorded in isolation

from the muscle action potential. It was thus shown that the endplate potential - unlike the action

potential - is a graded potential, since its amplitude varies with the strength of nerve fiber

stimulation.

Ultrastructural studies of the neuromuscular junction revealed the presence of numerous small

vesicles in the nerve terminal. These contain a signalling molecule (the neurotransmitter

acetylcholine, ACh). Upon arrival of an action potential at the nerve terminal the vesicles fuse

with the plasma membrane (exocytosis) and release their content, the Ach, into the extracellular

space between the nerve ending and the muscle surface (synaptic cleft). The neurotransmitter

subsequently diffuses to the postsynaptic muscle membrane and specifically binds to a receptor

protein that is heavily clustered at this site (acetylcholine receptor, AChR). The AChR is a

chemically gated ion channel that opens as soon as Ach has bound to it. As a consequence, cations

(mainly sodium) flow into the muscle cell, producing a small membrane depolarization, that

corresponds to the endplate potential described above. Finally, a muscle action potential is elicited

by voltage-gated sodium channels in the muscle membrane, opening in response to the endplate

potential. Synaptic transmission at a cholinergic synapse (like the neuromuscular junction) is

terminated by enzymatic degradation of the neurotransmitter by the enzyme acetylcholine-

esterase (AChE), which is localized in the postsynaptic membrane.Regulation of exocytosis and neurotransmitter release

The fusion of synaptic vesicles with the plasma membrane (exocytosis) is functionally linked to

the arrival of an action potential at the nerve ending by voltage-gated calcium channels. When these

channels open calcium ions flow into the nerve terminal, due to the steep concentration gradient.

This initiates a complex cascade of molecular activities that ultimately lead to the attachment of

synaptic vesicles to the presynaptic plama membrane and to fusion of the lipid bilayers:

In the resting state synaptic vesicles are docked to microfilaments within a nerve terminal

via a protein called synapsin. The rise in the intracellular calcium concentration induces a

conformational change in the synapsin protein, allowing synaptic vesicles to detach from the

microfilaments. In the next step vesicles become attached to the intracellular surface of the

presynaptic membrane. On the molecular level this is accomplished by the vesicle protein

synaptobrevin on the one side and the presynaptic membrane protein syntaxin on the other. Both

proteins align their α-helices in parallel to form a very compact and stable coiled-coil structure.

The ensuing formation of a fusion complex requires the presence of the presynaptic membrane

protein synaptotagmin which is believed to act as a calcium sensor. The proteins, which are

responsible to mediate vesicle fusion are the so-called SNAREs. They can be divided into two

categories: vesicle or v-SNAREs, which are incorporated into the membranes of transport vesicles

during budding, and target or t-SNAREs, which are associated with nerve terminal membranes.

Properties of Acetylcholine Receptors

Pharmacological properties

A most convenient way to characterize a neurotransmitter receptor in the living tissue is by studying

the effect of certain drugs on its physiological activity. Some drugs will mimic the effect of the

original neurotransmitter, they are called agonists. Others will block the physiological response

of the receptor even in the presence of the neurotransmitter, they are called antagonists. By testing

several agonists and antagonists it turned out that two different subtypes of acetylcholine

receptors occur in the skeletal and the heart muscle, respectively.

The AChR in the skeletal muscle is blocked by curare (antagonist) and activated by nicotine

(agonist), while those in the heart muscle is blocked by atropine and activated my muscarine,

instead. Both receptor subtypes are named according to their agonist: hence the skeletal muscle

receptor is called nicotinic AChR (nAChR), while those in heart is called muscarinic AChR

(mAChR).Structure and function of the nAChR protein

In order to characterize this protein biochemically, it was necessary to find a tissue that was highly

enriched in it (see also: isolation of the voltage-gated sodium channel). The electric organ of the

electric ray (Torpedo marmorata) proved as a most suitable source for isolating the nAChR. The

snake toxin peptide α−bungarotoxin helped to identify the receptor protein during the isolation

procedure. Biochemical studies ultimately showed that the nAChR is an oligomeric protein

consisting of four different polypeptides termed α,β,γ,δ. In the native protein complex the α-

subunit occurs twice, hence the AChR is a pentamer (i.e., it contains a total of five subunits) with

a stoichiometry of 2αβγδ. Since ACh binds to the α**-subunits**, each AChR can bind two molecules

of the neurotransmitter. The next step was the cloning of each of the four subunits by recombinant

DNA technology, allowing to deduce their amino acid sequences. Subsequent hydrophobicity

analysis revealed in each case four transmembrane segments (M1 –M4). By electron microscopy

the 3D-structure of the AChR was determined at least at low resolution. As was expected it forms

an ionic pore with a large extracellular funnel-like structure. The hydrophilic pore is lined by the

five M2 segments of the individual subunits. The two ACh-binding pockets are formed by the

extracellular portions extending from the M1 segments of the α− and γ**-** as well as the α**- and** δ**-**

subunits. Binding of two molecules of ACh induces a twisting movement within the M2-segments,

which opens the ionic pathway through the membrane.

Structure and function of the mAChR

While the nAChR is a chemically-gated ion channel (belonging to the family of ionotropic

receptors) the mAChR operates in a fundamentally different manner. First of all, it is not a pore-

forming protein, but consists of only a single subunit with seven transmembrane segments.

Secondly on the intracellular side it is linked to a GTP-binding protein (G-protein), a protein

complex of three different subunits (guanosine-triphosphate, GTP, is closely related adenosine-

triphosphate, ATP). The mAChR therefore is a member of the G-protein coupled receptor family

(also called metabotropic receptor family).

Binding of a single ACh molecule induces a conformational change in the receptor protein that

ultimately leads to a dissociation of the G-protein complex. The membrane anchored βγ**-subunit**

moves laterally within the membrane until it reaches a potassium channel to which it binds. The

channel is opened and the ensuing potassium efflux will hyperpolarize the postsynaptic membrane

thus creating an inhibitory postsynaptic potential (IPSP).Amino acid neurotransmitters

Besides acetylcholine certain amino acids can operate as neurotransmitters, as well. These are

glutamate, gamma-aminobutyric acid (GABA), and glycine. The family of glutamate receptors

comprises both metabotropic and ionotropic receptors. The former are G-protein coupled receptors

that come in at least eight different subtypes most of which induce ipsps. Ionotropic receptors can

be subdivided pharmacologically into NMDA-receptors (sensitive to the agonist N-methyl-D-

aspartate) and non-NMDA-receptors. As expected, non-NMDA-receptors are gated by glutamate

and due to the influx of sodium ions induce an excitatory postsynaptic potential. NMDA-receptors

by contrast are unresponsive to glutamate alone, since they have a magnesium block that keeps

their ionic pathway blocked. This block is removed by depolarization of the postsynaptic

membrane. Hence NMDA-receptors require membrane depolarization prior to or at least

concomitant with the release of glutamate since they are both chemically-gated and voltage-gated

ion channels. From this it is clear that synapses containing NMDA-receptors alone are

functionally silent. Hence NMDA-receptors normally co-localize and co-operate with non-

NMDA-receptors at glutamatergic synapses. Another striking feature of NMDA-receptors is their

high permeability for calcium. Influx of calcium trough NMDA-receptors elicits postsynaptic

activities leading to a use-dependent change of synaptic efficiency as observed during learning

processes (see chapter “Synaptic Plasticity”).

As compared with the nicotinic AChR ionotropic glutamate receptors slightly deviate in

their membrane topology, in that they possess only three transmembrane segments that are

connected via a hairpin loop element resembling those found in voltage-gated potassium channels.

GABA-receptors comprise ionotropic and metabotropic receptors as well. The former are

called GABA

A**-receptors** while the latter are termed GABA

B**-receptors**. GABA

B-receptors have

seven transmembrane domains and similar as metabotropic AChR open K+

-channels via the

liberated βγ-subunits of G-proteins, ultimately leading to an ipsp.

GABA

A-receptors are chemically-gated chloride channels, which induce ipsps via a chloride

influx into the postsynaptic cells**.** In their basic structural arrangement, they closely resemble

ionotropic AChR in that they are composed of five subunits (pentamer) each of which possesses

four transmembrane segments.

The involvement of GABA-receptors in a neuronal circuit is most conveniently

demonstrated by the application of specific drugs. The plant toxin bicuculline is a specific

GABAergic antagonist that competes with GABA for its binding pocket. In living organismsit causes severe convulsions since it abolishes all inhibitory synaptic activity.

Alternatively, the toxin picrotoxin is frequently used which directly binds to the ion channel

portion of the GABA-receptor and not to its binding pocket. Hence it is called an allosteric

antagonist.

Furthermore, GABAA-receptors are the targets for a variety of therapeutically relevant drugs such

as barbiturates (components of sleeping pills) and benzodiazepines (“Valium”) which act as

allosteric agonists enhancing the effect of GABA. Since these drugs all increase synaptic

inhibition in the brain, they have a sedative or even anesthetic effect in living organisms.

Glycine-receptors closely resemble GABAA-receptors. They are also chemically-gated chloride

channels and exhibit a similar overall molecular structure. They are more abundant in spinal cord

tissue than in brain.

Biogenic Amines

Biogenic amines form another important class of neurotransmitter molecules. They are produced

by nerve cells using the amino acid tyrosine as starting material. By enzymatic removal of the

acidic group (-COOH) and subsequent addition of a hydroxyl group (-OH) the neurotransmitter

dopamine is generated. Dopamine binds to G-protein coupled receptors D1-D5. The level of

dopamine available in nerve terminals is controlled by the enzyme monoamineoxidase (MAO),

which inactivates the neurotransmitter in the presynapse. Dopaminergic neurons are most abundant

in two midbrain regions, the substantia nigra (“black nucleus”) and the ventral tegmental area. The

latter is part of the mesolimbic dopaminergic pathway that is involved in the processing of

rewarding stimuli and drug addiction. Dopamine receptors are also important targets of

antipsychotic drugs. Furthermore, one of the most widespread neurodegenerative diseases,

parkinsonism, is caused by a gradual degeneration of dopaminergic neurons in the substantia nigra.

The second member of this group, noradrenaline (= norepinephrine) is generated from

dopamine by the addition of another hydroxyl group (-OH). Neurons in the locus coeruleus (“blue

nucleus”) represent a major source of noradrenaline in the brain. They send out numerous axon

collaterals into the thalamus and throughout the cortex. The widespread distribution of

noradrenergic nerve terminals in the forebrain explains the profound influence of noradrenaline

on a variety of higher brain functions including multimodal alertness and motivation.Electrical Synapses

In contrast with chemical synapses that use a neurotransmitter substance to pass over neuronal

signals to a target cell electrical synapses directly convey signals from one cell to the other. Hence,

they do not have synaptic vesicles and the extracellular space between pre-and postsynaptic

membrane is greatly diminished. Direct electrical coupling of pre-and postsynaptic membranes is

achieved by densely packed membrane channels, which allow an unimpeded passage of charged

or uncharged particles up to a size of approx. 1000 daltons molecular weight. These channels,

termed connexons are formed by six subunits of the protein connexin, which is a four

transmembrane domain protein. Electrical synapses operate more quickly than chemical synapses

and, in many cases, allow current flow in both directions. As a whole they provide a means to

synchronize electrical signalling in a network of neurons.

Synaptic Integration

Nerve cells generate action potentials at a specific site, the axon initial segment. In this region the

threshold to fire an action potential is lowest, probably due to a strong accumulation of voltage-

gated sodium channels there. If a single epsp is elicited at a synapse somewhere on a dendrite this

local depolarization will passively spread across the neuronal membrane to finally reach the axon

hillock. Since on its way much of its original voltage will decay, a single epsp usually will not

suffice to overcome the firing threshold at the axon hillock. If several epsps occur in fast succession

at a synapse (temporal summation) the depolarizations may superimpose thus greatly increasing

the chance to generate an action potential at the axon hillock. Alternatively, several epsps might be

generated simultaneously at various synapses (spatial summation) to overcome the firing

threshold there. As a whole, the somatic and dendritic membrane surface of a nerve cells serves to

integrate all synaptic potentials arriving at a time to ultimately decide if the target cell itself will

elicit an action potential or not. In this complex process not only epsps but also ipsps have to be

considered.

Synaptic Plasticity

The ability of synapses to change their response to incoming signals in a use-dependent manner is

called synaptic plasticity. It is typically accompanied by an increase (or decrease) in the size of

the epsp generated in response to a given stimulation. In pioneering experiments, it was found that

the epsps of a synapse significantly increase after high frequency stimulation(posttetanic potentiation). The effect, however, lasts for only a few minutes. It is due to an

accumulation of calcium in the nerve terminal during tetanic stimulation.

In more sophisticated experiments performed by the laboratory of Eric Kandel the molecular

basis of synaptic plasticity was investigated. By using the sea hare (Aplysia californica) as a model

organism they could throw a bridge between a “learned” animal behaviour and the underlying

cellular and molecular processes. The gills of the sea hare (actually a snail!) are very sensitive to

mechanical stimulation and quickly retract when being touched (gill withdrawal reflex). Repeated

weak stimulation of this kind, however, gradually attenuates the response (a process called

habituation). If the habituated animal receives a strong, even toxic stimulus of the antennae, the

gill withdrawal response gets sensitized. This can be explained by the wiring of sensory fibers in

the Aplysia nervous system. The sensory fibers from the antennae make axo-axonic synapses on

the nerve terminals of sensory fibers coming from the gills. These synapses use serotonin as

neurotransmitter**. Serotonin** release activates the G-protein coupled serotonin receptor at the

postsynapse (which is the nerve terminal membrane of the “gill fibers”). As usual for G-protein

coupled receptors, the G-protein subsequently dissociates, releasing α- as well as βγ-subunits. The

further chain of events is as follows:

• G-protein α-subunits activate the enzyme adenylyl cyclase.

• the enzymes start to produce cyclic adenosine monophosphate (cAMP) from ATP

• cAMP activates the enzyme protein kinase A

• protein kinase A phosphorylates potassium channels, leading to current reduction.

• the repolarization of action potentials arriving at the “gill fiber” synapse is delayed.

• neurotransmitter release is enhanced.

As long as the potassium channels retain phosphorylation synaptic transmission between the gill

sensory fiber and the motoneuron activating the gill muscle is enhanced.

Studies with Mutant Flies

The fruit fly Drosophila has proven as a most convenient model organism to analyze the molecular

basis of cellular processes, since mutations can be rather conveniently generated and isolated.

Learning mutants (“stupid flies”) were identified by an odour discrimination task. It was found

that deficits in this learning task in many cases correlated with mutations of genes encoding proteins

controlling the cAMP-level, such as adenylyl cyclase (AC, increases the level of cAMP) or

phosphodiesterase (PDE, decreases the level of cAMP), emphasizing the key role of cyclic AMP

in learning processes. More recently is was found that cAMP inaddition to its effect on ion channel phosphorylation (se above) can also affect gene expression

through its binding to the regulatory parts of transcription factors in the cell nucleus. This could

lead to long term changes in the nervous system such as the new outgrowth of nerve fibers and

the formation of additional synapses.

Long term Potentiation

The hippocampus is a forebrain structure (telencephalon) that is closely associated with long term

memory formation, since its removal abolishes declarative memory formation in humans.

Therefore, this brain region has become a model system to analyze the cellular and molecular basis

of learning processes in higher animal species. Since the majority of internal connections of

hippocampal neurons are arranged within a plane it is possible to cut out tissue sections (< 1/2 mm

thick) from the hippocampus without damaging its internal circuitry. Owing to the highly ordered

arrangement of neurons in discrete layers electrophysiological recording of defined cells within a

tissue section is feasible. Most frequently the synaptic connections between CA3 and CA1

neurons are being studied (CA stands for cornu ammonis = ammons horn). CA3 cells are

connected with CA1 neurons through the so-called Schaffer collaterals, the nerve terminals of

which are excitatory and release glutamate. The pioneering observation was made in 1973 by

Bliss and Lomo who showed that a high-frequency stimulation of Schaffer collaterals produces a

significant increase in the epsp. Since the effect lasts for hours it is called long term potentiation

(LTP). On a molecular level NMDA-receptors play a key role in the induction of LTP. As outlined

above (chapter amino acid neurotransmitters) these receptors require postsynaptic membrane

depolarization that removes a Mg

2+

-block to become responsive to glutamate. High-frequency

stimulation evokes depolarization of an extended portion of the dendritic tree of CA1 neurons.

Under these conditions glutamate release from Schaffer collateral synapses coincides with

postsynaptic membrane depolarization. The NMDA-receptor hence can be considered as a

coincidence detector molecule. Since NMDA-receptor ion channels are permeable to calcium the

calcium concentration in the postsynaptic cell increases. Calcium acts as second messenger that

induces several metabolic effects in the target cell:

1. Postsynaptic effects:

Calcium activates an enzyme called calcium-calmodulin kinase II (CaM-kinase II). This

enzyme first of all phosphorylates itself (autophosphorylation) which stabilizes its own

activated state (explaining the long-term effect of LTP). Secondly it induces the insertionof additional non-NMDA receptors into the postsynaptic membrane, leading to an increase in

the epsp even after a weaker stimulation.

  1. Presynaptic effects:

Calcium additionally activates an enzyme that produces the gaseous neurotransmitter nitric

oxide (NO). Gases like NO can easily penetrate membranes and hence can reach the

presynaptic nerve terminal (retrograde messenger). NO is believed to enhance

neurotransmitter release by still unknown mechanisms.

Basic Architecture of the Spinal Cord

The spinal cord is part of the central nervous system. It is surrounded by the vertebral column

and exhibits a segmental organization. The spinal cord is connected to its target areas on the body

surface by peripheral nerves. On cross sections a central grey matter, harbouring most of the

neurons, is surrounded by white matter largely consisting of myelinated nerve fibers. On the dorsal

side pairs of ganglia occur (dorsal root ganglia) that contain the cell bodies of pseudo-unipolar

ganglion cells. These send out long sensory fibers into the skin, muscles, and joints to detect

mechanical stimuli, such as touch, stretch, pain, and temperature. Sensory signals are

subsequently transferred by the axons of pseudo-unipolar cells into the grey matter of spinal cord

via the dorsal roots. In many cases the information is directly targeted to motoneurons residing

in the ventral part of the grey matter (ventral horn). If their axons project back to muscles of the

body region that had been previously stimulated a reflex arc is activated. Owing to this direct

connection between sensory input and motor output, often involving only a single synaptic

contact, reflexes are very fast and cannot be influenced voluntarily. The knee jerk is a famous

example for such a monosynaptic reflex. It is initiated by a week hammer hit on the surface of the

patella. A slight dislocation of this bone pulls the tendon to which it is connected. This activates a

sensory structure (stretch receptor) within the adjoining muscle. The stretch signal enters the spinal

cord via the dorsal roots as described above and is directly transferred onto a motoneuron that

activates the extensor muscle in the leg. To rule out concomitant activation of the antagonistic

flexor muscle motoneurons commanding this muscle are inhibited by the same signal via a

circuitry called afferent collateral inhibition (for details see transparency).

Ascending and descending connections

In addition to this local processing of signals on the level of a single spinal cord segment there are

extensive connections with the brain, in particular with cortical areas involved in voluntary

movement control (motor cortex). These are provided by ascending anddescending pathways that exhibit a specific and highly ordered arrangement in the white matter:

ascending fibers transporting sensory signals related to temperature and pain traverse the midline

of the spinal cord to ascend on the opposite side (contralateral projection) to the brain, while

those conveying signals about touch remain on the same side (ipsilateral projection). Descending

fibers from the motor cortex are also connected in an ipsilateral fashion. As a result, a half-sided

transection of the spinal cord produces the so-called Brown-Séquard syndrome, which is

typically evoked by motor cycle accidents. In this syndrome the injured person suffers from

paralysis and loss of touch sensation in the leg of the injured side, while it experiences loss of

temperature and pain sensation in the opposite leg.

Rhythmic movement control

In addition to the execution of reflexes the spinal cord plays an important role in regulating

rhythmic movements such as swimming, walking, and running, thus relieving higher brain

regions from detailed movement control (servo function). Rhythmic movements are typically

based on a periodic and alternating activation of antagonist muscle groups of a limb. This periodic

activity can be traced back to the activity of corresponding neurons in the ventral roots which show

a wiring diagram that is designed to create periodic activity patterns (half-centre model, for details

see transparency).

The central pattern generator of the spinal cord can be even nailed down to the molecular level.

By the coordinated activity of certain ion channels a periodic interruption of action potential firing

is provided: thereby the concerted interaction of voltage-gated calcium-channels and calcium-

activated potassium channels plays a key role (for details see transparency).

The Autonomic Nervous System

The autonomic nervous system controls the activity of inner organs such as heart, lung, stomach,

liver etc. It operates independently from voluntary control and is of key relevance for the survival

of an organism since it coordinates vital visceral activities such as digestion, heart beat or the

control of body temperature. Structurally it is closely interlocked with the spinal cord and

peripheral nerves and it exhibits also a reflex arc organization. As compared with the above-

mentioned somatic reflex arc an autonomic reflex arc exhibits the following specializations:• the cell bodies of the autonomic neurons in the spinal cord are localized in the intermediate

region of grey matter. Their axons leave the spinal cord via the ventral roots joining spinal

nerves.

• their axons do not project directly to the target organs but terminate in autonomic ganglia

first

• from there so-called postganglionic fibers emanate to contact a certain inner organ

• each inner organ receives a dual innervation through both a sympathetic and a

parasympathetic branch.

• dual innervation allows for a better fine-tuning, coordination, and adaptation of inner organ

activities to changing environmental and emotional conditions.

• typically, those organs preparing the organism for fight and flight are activated by the

sympathetic branch and inhibited by the parasympathetic branch.

• organs preparing the organism for rest and digest are activated by the parasympathetic

pathway and inhibited by the sympathetic pathway.

The sympathetic ganglia are lined up as a chain along the spinal cord. Parasympathetic ganglia

usually lie close to the target organ, instead.

Sympathetic ganglia occur in the breast and lumbal region of the spinal cord, while

parasympathetic fibers emanate from the nucleus of the nervus vagus in the brainstem as well as

from the sacral region of spinal cord.

In the parasympathetic pathway both preganglionic and postganglionic fibers are

cholinergic. The target neurons of the former possess nicotinic AChRs, while the targets of the

latter use muscarinic AChRs, instead.

In the sympathetic pathway preganglionic fibres release acetylcholine which binds to nicotinic

AChRs. Postganglionic fibers use noradrenaline instead.

The third branch of the autonomic nervous system is the enteric nervous system (ENS). The

enteric nervous system (ENS) is large, complex and uniquely able to orchestrate gastrointestinal

behaviour independently of the central nervous system (CNS). It is situated within the wall of the

gastrointestinal tract and in human contains 200-600 million neurons, distributed in many thousands

of small ganglia, the great majority of which are found in two plexuses, the myenteric and

submucosal plexuses.

The myenteric plexus forms a continuous network that extends from the upper esophagus to

the internal anal sphincter and is located between the longitudinal and circular layers of muscle.Submucosal ganglia and connecting fiber bundles form plexuses in the small and large

intestines buried in the submucosa, but not in the stomach and esophagus.

see also

Tags: neurobiology science
Superlink: 051 ☣Neurobiology 050 🧠Neuroscience
Intro to Neurobiology Deck

Source

Created: 20-07-24 15:43