Literature DB >> 10212476

Multitude of ion channels in the regulation of transmitter release.

R Rahamimoff1, A Butkevich, D Duridanova, R Ahdut, E Harari, S G Kachalsky.   

Abstract

The presynaptic nerve terminal is of key importance in communication in the nervous system. Its primary role is to release transmitter quanta on the arrival of an appropriate stimulus. The structural basis of these transmitter quanta are the synaptic vesicles that fuse with the surface membrane of the nerve terminal, to release their content of neurotransmitter molecules and other vesicular components. We subdivide the control of quantal release into two major classes: the processes that take place before the fusion of the synaptic vesicle with the surface membrane (the pre-fusion control) and the processes that occur after the fusion of the vesicle (the post-fusion control). The pre-fusion control is the main determinant of transmitter release. It is achieved by a wide variety of cellular components, among them the ion channels. There are reports of several hundred different ion channel molecules at the surface membrane of the nerve terminal, that for convenience can be grouped into eight major categories. They are the voltage-dependent calcium channels, the potassium channels, the calcium-gated potassium channels, the sodium channels, the chloride channels, the non-selective channels, the ligand gated channels and the stretch-activated channels. There are several categories of intracellular channels in the mitochondria, endoplasmic reticulum and the synaptic vesicles. We speculate that the vesicle channels may be of an importance in the post-fusion control of transmitter release.

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Year:  1999        PMID: 10212476      PMCID: PMC1692499          DOI: 10.1098/rstb.1999.0379

Source DB:  PubMed          Journal:  Philos Trans R Soc Lond B Biol Sci        ISSN: 0962-8436            Impact factor:   6.237


  114 in total

1.  Kinetics, Ca2+ dependence, and biophysical properties of integrin-mediated mechanical modulation of transmitter release from frog motor nerve terminals.

Authors:  B M Chen; A D Grinnell
Journal:  J Neurosci       Date:  1997-02-01       Impact factor: 6.167

Review 2.  Pre- and postfusion regulation of transmitter release.

Authors:  R Rahamimoff; J M Fernandez
Journal:  Neuron       Date:  1997-01       Impact factor: 17.173

3.  Exo-endocytosis and closing of the fission pore during endocytosis in single pituitary nerve terminals internally perfused with high calcium concentrations.

Authors:  H Rosenboom; M Lindau
Journal:  Proc Natl Acad Sci U S A       Date:  1994-06-07       Impact factor: 11.205

4.  Localization of calcium signals by a mobile calcium buffer in frog saccular hair cells.

Authors:  W M Roberts
Journal:  J Neurosci       Date:  1994-05       Impact factor: 6.167

5.  Activation and inactivation of the bursting potassium channel from fused Torpedo synaptosomes.

Authors:  J Edry-Schiller; R Rahamimoff
Journal:  J Physiol       Date:  1993-11       Impact factor: 5.182

6.  Clustering of Ca2+ channels and Ca(2+)-activated K+ channels at fluorescently labeled presynaptic active zones of hair cells.

Authors:  N P Issa; A J Hudspeth
Journal:  Proc Natl Acad Sci U S A       Date:  1994-08-02       Impact factor: 11.205

7.  Identification and function of glycine receptors in cultured cerebellar granule cells.

Authors:  P Wahl; L Elster; A Schousboe
Journal:  J Neurochem       Date:  1994-06       Impact factor: 5.372

8.  Hormone release from isolated nerve endings of the rat neurohypophysis.

Authors:  M Cazalis; G Dayanithi; J J Nordmann
Journal:  J Physiol       Date:  1987-09       Impact factor: 5.182

9.  Cholinergic vesicle specific proteoglycan: stability in isolated vesicles and in synaptosomes during induced transmitter release.

Authors:  D M Kuhn; W Volknandt; H Stadler; H Zimmermann
Journal:  J Neurochem       Date:  1988-01       Impact factor: 5.372

Review 10.  Molecular and cellular physiology of intracellular calcium stores.

Authors:  T Pozzan; R Rizzuto; P Volpe; J Meldolesi
Journal:  Physiol Rev       Date:  1994-07       Impact factor: 37.312

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  2 in total

1.  Isoflurane inhibits synaptic vesicle exocytosis through reduced Ca2+ influx, not Ca2+-exocytosis coupling.

Authors:  Joel P Baumgart; Zhen-Yu Zhou; Masato Hara; Daniel C Cook; Michael B Hoppa; Timothy A Ryan; Hugh C Hemmings
Journal:  Proc Natl Acad Sci U S A       Date:  2015-09-08       Impact factor: 11.205

Review 2.  Regulation of cell function by methionine oxidation and reduction.

Authors:  T Hoshi; S Heinemann
Journal:  J Physiol       Date:  2001-02-15       Impact factor: 5.182

  2 in total

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