An axon terminal (A) transmits a signal to neuron B (receiving). Features: 1.Mitochondrion. 2.Synaptic vesicle filled with neurotransmitter molecules. 3. Autoreceptor. 4.Synaptic cleft with neurotransmitter molecules. 5. Postsynaptic receptors activated by neurotransmitters (induction of a postsynaptic potential). 6.Calcium channel. 7. Exocytosis of a vesicle. 8. Recaptured neurotransmitter.
Axon terminals (also called synaptic boutons, presynaptic terminals, or end-feet) are distal terminations of the branches of an axon. An axon, also called a nerve fiber, is a long, slender projection of a nerve cell that conducts electrical impulses called action potentials away from the neuron's cell body to transmit those impulses to other neurons, muscle cells, or glands. Most presynaptic terminals in the central nervous system are formed along the axons (en-passant boutons), not at their ends (terminal boutons).
Functionally, the axon terminal converts an electrical signal into a chemical signal. When an action potential arrives at an axon terminal (A), the neurotransmitter is released and diffuses across the synaptic cleft. If the postsynaptic cell (B) is also a neuron, neurotransmitter receptors generate a small electrical current that changes the postsynaptic potential. If the postsynaptic cell (B) is a muscle cell (neuromuscular junction), it contracts.
Axon terminals are specialized to release neurotransmitters very rapidly by exocytosis.[1] Neurotransmitter molecules are packaged into synaptic vesicles that cluster beneath the axon terminal membrane on the presynaptic side (A) of a synapse. Some of these vesicles are docked, i.e., connected to the membrane by several specialized proteins, such as the SNARE complex. The incoming action potential activates voltage-gated calcium channels, leading to an influx of calcium ions into the axon terminal. The SNARE complex reacts to these calcium ions. It forces the vesicle's membrane to fuse with the presynaptic membrane, releasing their content into the synaptic cleft within 180 μs of calcium entry.[2][3][4] When receptors in the postsynaptic membrane bind this neurotransmitter and open ion channels, information is transmitted between neurons (A) and neurons (B).[5] To generate an action potential in the postsynaptic neuron, many excitatory synapses must be active at the same time.[1]
Historically, calcium-sensitive dyes were the first tool to quantify the calcium influx into synaptic terminals and to investigate the mechanisms of short-term plasticity.[6] The process of exocytosis can be visualized with pH-sensitive fluorescent proteins (Synapto-pHluorin): Before release, vesicles are acidic, and the fluorescence is quenched. Upon release, they are neutralized, generating a brief flash of green fluorescence.[7] Another possibility is constructing a genetically encoded sensor that becomes fluorescent when bound to a specific neurotransmitter, e.g., glutamate.[8] This method is sensitive enough to detect the fusion of a single transmitter vesicle in brain tissue and to measure the release probability at individual synapses.[9]
^Rizo J (August 2018). "Mechanism of neurotransmitter release coming into focus". Protein Science (Review). 27 (8): 1364–1391. doi:10.1002/pro.3445. PMC6153415. PMID29893445. Research for three decades and major recent advances have provided crucial insights into how neurotransmitters are released by Ca2+ -triggered synaptic vesicle exocytosis, leading to reconstitution of basic steps that underlie Ca2+ -dependent membrane fusion and yielding a model that assigns defined functions for central components of the release machinery.
^Siegelbaum, Steven A. (2021). Kandel, Eric R.; Koester, John D.; Mack, Sarah H. (eds.). Principles of neural science (6th ed.). New York: McGraw-Hill. ISBN978-1-259-64223-4.
Vaquero CF, de la Villa P (October 1999). "Localisation of the GABA(C) receptors at the axon terminal of the rod bipolar cells of the mouse retina". Neuroscience Research. 35 (1): 1–7. doi:10.1016/S0168-0102(99)00050-4. PMID10555158. S2CID53189471.
Roffler-Tarlov S, Beart PM, O'Gorman S, Sidman RL (May 1979). "Neurochemical and morphological consequences of axon terminal degeneration in cerebellar deep nuclei of mice with inherited Purkinje cell degeneration". Brain Research. 168 (1): 75–95. doi:10.1016/0006-8993(79)90129-X. PMID455087. S2CID19618884.
Yagi T, Kaneko A (February 1988). "The axon terminal of goldfish retinal horizontal cells: a low membrane conductance measured in solitary preparations and its implication to the signal conduction from the soma". Journal of Neurophysiology. 59 (2): 482–494. doi:10.1152/jn.1988.59.2.482. PMID3351572.
LTP promotes formation of multiple spine synapses between a single axon terminal and a dendrite.Toni N, Buchs PA, Nikonenko I, Bron CR, Muller D (November 1999). "LTP promotes formation of multiple spine synapses between a single axon terminal and a dendrite". Nature. 402 (6760): 421–425. Bibcode:1999Natur.402..421T. doi:10.1038/46574. PMID10586883. S2CID205056308.
