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New Insights Into Interactions of Presynaptic Calcium Channel Subtypes and SNARE Proteins in Neurotransmitter Release
Action potential (AP) induces presynaptic membrane depolarization and subsequent opening of Ca(2+) channels, and then triggers neurotransmitter release at the active zone of presynaptic terminal. Presynaptic Ca(2+) channels and SNARE proteins (SNAREs) interactions form a large signal transfer comple...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054978/ https://www.ncbi.nlm.nih.gov/pubmed/30061813 http://dx.doi.org/10.3389/fnmol.2018.00213 |
Sumario: | Action potential (AP) induces presynaptic membrane depolarization and subsequent opening of Ca(2+) channels, and then triggers neurotransmitter release at the active zone of presynaptic terminal. Presynaptic Ca(2+) channels and SNARE proteins (SNAREs) interactions form a large signal transfer complex, which are core components for exocytosis. Ca(2+) channels serve to regulate the activity of Ca(2+) channels through direct binding and indirect activation of active zone proteins and SNAREs. The activation of Ca(2+) channels promotes synaptic vesicle recruitment, docking, priming, fusion and neurotransmission release. Intracellular calcium increase is a key step for the initiation of vesicle fusion. Various voltage-gated calcium channel (VGCC) subtypes exert different physiological functions. Until now, it has not been clear how different subtypes of calcium channels integrally regulate the release of neurotransmitters within 200 μs of the AP arriving at the active zone of synaptic terminal. In this mini review, we provide a brief overview of the structure and physiological function of Ca(2+) channel subtypes, interactions of Ca(2+) channels and SNAREs in neurotransmitter release, and dynamic fine-tune Ca(2+) channel activities by G proteins (Gβγ), multiple protein kinases and Ca(2+) sensor (CaS) proteins. |
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