دورية أكاديمية
أعرض في EDS

Are unreliable release mechanisms conserved from NMJ to CNS?

التفاصيل البيبلوغرافية
العنوان: Are unreliable release mechanisms conserved from NMJ to CNS?
المؤلفون: Tarr TB; Department of Neuroscience, Center for Neuroscience, University of Pittsburgh, Pittsburgh, PA 15260, USA., Dittrich M, Meriney SD
المصدر: Trends in neurosciences [Trends Neurosci] 2013 Jan; Vol. 36 (1), pp. 14-22. Date of Electronic Publication: 2012 Oct 25.
نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.; Review
اللغة: English
بيانات الدورية: Publisher: Elsevier Applied Science Publishing Country of Publication: England NLM ID: 7808616 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-108X (Electronic) Linking ISSN: 01662236 NLM ISO Abbreviation: Trends Neurosci Subsets: MEDLINE
أسماء مطبوعة: Publication: Barking : Elsevier Applied Science Publishing
Original Publication: Amsterdam, New York, Elsevier/North-Holland Biomedical Press.
مواضيع طبية MeSH: Central Nervous System/*physiology , Neuromuscular Junction/*physiology , Synapses/*physiology , Synaptic Transmission/*physiology, Animals ; Humans
مستخلص: The frog neuromuscular junction (NMJ) is a strong and reliable synapse because, during activation, sufficient neurotransmitter is released to trigger a postsynaptic action potential (AP). Recent evidence supports the hypothesis that this reliability emerges from the assembly of thousands of unreliable single vesicle release sites. The mechanisms that govern this unreliability include a paucity of voltage-gated calcium channels, a low probability of calcium channel opening during an AP, and the rare triggering of synaptic vesicle fusion even when a calcium channel does open and allows calcium flux. Here, we discuss the evidence that these unreliable single vesicle release sites may be the fundamental building blocks of many types of synapses in both the peripheral and central nervous system (PNS and CNS, respectively).
(Copyright © 2012 Elsevier Ltd. All rights reserved.)
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معلومات مُعتمدة: P41 GM103712 United States GM NIGMS NIH HHS; P41 RR006009 United States RR NCRR NIH HHS; P41RR06009 United States RR NCRR NIH HHS
تواريخ الأحداث: Date Created: 20121030 Date Completed: 20130722 Latest Revision: 20211021
رمز التحديث: 20221213
مُعرف محوري في PubMed: PMC4076818
DOI: 10.1016/j.tins.2012.09.009
PMID: 23102681
قاعدة البيانات: MEDLINE
الوصف
تدمد:1878-108X
DOI:10.1016/j.tins.2012.09.009