Synapse

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This article is about a part of the nervous system. For other uses see Synapse (disambiguation).

Synapses are specialized junctions through which cells of the nervous system signal to one another and to non-neuronal cells such as muscles or glands. A synapse between a motor neuron and a muscle cell is called a neuromuscular junction.

Synapses allow the neurons of the central nervous system to form interconnected neural circuits. They are thus crucial to the biological computations that underlie perception and thought. They also provide the means through which the nervous system connects to and controls the other systems of the body.

The human brain contains a huge number of synapses, with young children having about 1,000 trillion. This number declines with age, stabilizing by adulthood. Estimates for an adult vary from 100 to 500 trillion synapses.

The word "synapse" comes from "synaptein" which Sir Charles Scott Sherrington and his colleagues coined from the Greek "syn-" meaning "together" and "haptein" meaning "to clasp".

1 Anatomy
2 Signaling across chemical synapses
3 Synaptic strength
4 Integration of synaptic inputs
5 Detailed properties and regulation
6 Immunological synapses
7 References
8 External links

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Anatomy

At a prototypical synapse, such as those found at dendritic spines, a mushroom-shaped bud projects from each of two cells and the caps of these buds press flat against one another. At this interface, the membranes of the two cells flank each other across a slender gap, the narrowness of which enables signalling molecules known as neurotransmitters to pass rapidly from one cell to the other by diffusion. This gap, which is about 20 nm wide, is known as the synaptic cleft.

Such synapses are asymmetric both in structure and in how they operate. Only the so-called pre-synaptic neuron secretes the neurotransmitter, which binds to receptors facing into the synapse from the post-synaptic cell. The pre-synaptic nerve terminal (also called the synaptic button or bouton) generally buds from the tip of an axon, while the post-synaptic target surface typically appears on a dendrite, a cell body, or another part of a cell. The parts of synapses where neurotransmitter is released are called the active zones. At active zones the membranes of the two adjacent cells are held in close contact by cell adhesion proteins. Immediately behind the post-synaptic membrane is an elaborate complex of interlinked proteins called the postsynaptic density. Proteins in the postsynaptic density serve a myriad of roles, from anchoring and trafficking neurotransmitter receptors into the plasma membrane, to anchoring various proteins which modulate the activity of the receptors. The postsynaptic cell need not be a neuron. Postsynaptic cells can also be gland or muscle cells.

There also exists a less elaborate form of junction called an electrical synapse, in which neurons are electrically coupled to each other via protein complexes called gap junctions.

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Signaling across chemical synapses

The release of neurotransmitter is triggered by the arrival of a nerve impulse (or action potential) and occurs through an unusually rapid process of cellular secretion: Within the pre-synaptic nerve terminal, vesicles containing neurotransmitter sit "docked" and ready at the synaptic membrane. The arriving action potential produces an influx of calcium ions through voltage-dependent, calcium-selective ion channels. Calcium ions then trigger a biochemical cascade which results in vesicles fusing with the presynaptic-membrane and release their contents to the synaptic cleft. Receptors on the opposite side of the synaptic gap bind neurotransmitter molecules and respond by opening nearby ion channels in the post-synaptic cell membrane, causing ions to rush in or out and changing the local transmembrane potential of the cell. The resulting change in voltage is called a postsynaptic potential. The result is excitatory, in the case of depolarizing currents, or inhibitory in the case of hyperpolarizing currents. Whether a synapse is excitatory or inhibitory depends on what type(s) of ion channel conduct the post-synaptic current, which in turn is a function of the type of receptors and neurotransmitter employed at the synapse.

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Synaptic strength

The strength of a synapse is defined by the change in transmembrane potential resulting from activation of the postsynaptic neurotransmitter receptors. This change in voltage is known as a post-synaptic potential, and is a direct result of ionic currents flowing through the post-synaptic receptor-channels. Changes in synaptic strength can be short-term and without permanent structural changes in the neurons themselves, lasting seconds to minutes - or long-term (long-term potentiation, or LTP), in which repeated or continuous synaptic activation can result in second messenger molecules initiating protein synthesis in the neuron's nucleus, resulting in alteration of the structure of the neuron itself. Learning and memory are believed to result from long-term changes in synaptic strength, via a mechanism known as synaptic plasticity.

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Integration of synaptic inputs

Generally, if an excitatory synapse is strong, an action potential in the pre-synaptic neuron will trigger another in the post-synaptic cell; whereas at a weak synapse the excitatory post-synaptic potential ("EPSP") will not reach the threshold for action potential initiation. In the brain, however, each neuron typically connects or synapses to many others, and likewise each receives synaptic inputs from many others. When action potentials fire simultaneously in several neurons that weakly synapse on a single cell, they may initiate an impulse in that cell even though the synapses are weak. On the other hand, a pre-synaptic neuron releasing an inhibitory neurotransmitter such as GABA can cause inhibitory postsynaptic potential in the post-synaptic neuron, decreasing its excitability and therefore decreasing the neuron's likelihood to fire an action potential. In this way the output of a neuron may depend on the input of many others, each of which may have a different degree of influence, depending on the strength of its synapse with that neuron. John Carew Eccles performed some of the important early experiments on synaptic integration, for which he received the Nobel Prize for Physiology or Medicine in 1963. Complex input/output relationships form the basis of transistor-based computations in computers, and are thought to figure similarly in neural circuits.

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Detailed properties and regulation

Following fusion of the synaptic vesicles and release of transmitter molecules into the synaptic cleft, the neurotransmitter is rapidly cleared from the space for recycling by specialized membrane proteins in the pre-synaptic or post-synaptic membrane. This "re-uptake" prevents "desensitization" of the post-synaptic receptors and ensures that succeeding action potentials will elicit the same size EPSP. The necessity of re-uptake and the phenomenon of desensitization in receptors and ion channels means that the strength of a synapse may in effect diminish as a train of action potentials arrive in rapid succession--a phenomenon that gives rise to the so-called frequency dependence of synapses. The nervous system exploits this property for computational purposes, and can tune its synapses through such means as phosphorylation of the proteins involved. The size, number and replenishment rate of vesicles also are subject to regulation, as are many other elements of synaptic transmission. For example, a class of drugs known as selective serotonin re-uptake inhibitors or SSRIs affect certain synapses by inhibiting the re-uptake of the neurotransmitter serotonin. In contrast, one important excitatory neurotransmitter, acetylcholine, does not undergo re-uptake, but instead is removed from the synapse by the action of the enzyme acetylcholinesterase.

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Immunological synapses

By analogy to true synapses described above, the interface between an antigen-presenting cell and lymphocyte is sometimes called an immunological synapse.

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References

M.F. Bear, B.W. Connors, and M.A. Paradiso. 2001. Neuroscience: Exploring the Brain. Baltimore: Lippincott. ISBN 0781739446
Kandel ER, Schwartz JH, Jessell TM. Principles of Neural Science, 4th ed. McGraw-Hill, New York (2000). ISBN 0838577016
J.G. Nicholls, A.R. Martin, B.G. Wallace and P.A. Fuchs. "From Neuron to Brain". 4th ed. Sinauer Associates, Sunderland, MA. ISBN 0878924391

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