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神经营养因子在神经递质释放中的作用。

The role of neurotrophins in neurotransmitter release.

作者信息

Tyler William J, Perrett Stephen P, Pozzo-Miller Lucas D

机构信息

Department of Psychology, Civitan International Research Center. University of Alabama at Birmingham, Birmingham, Alabama 35294-0021, USA.

出版信息

Neuroscientist. 2002 Dec;8(6):524-31. doi: 10.1177/1073858402238511.

Abstract

The neurotrophins (NTs) have recently been shown to elicit pronounced effects on quantal neurotransmitter release at both central and peripheral nervous system synapses. Due to their activity-dependent release, as well as the subcellular localization of both protein and receptor, NTs are ideally suited to modify the strength of neuronal connections by "fine-tuning" synaptic activity through direct actions at presynaptic terminals. Here, using BDNF as a prototypical example, the authors provide an update of recent evidence demonstrating that NTs enhance quantal neurotransmitter release at synapses through presynaptic mechanisms. The authors further propose that a potential target for NT actions at presynaptic terminals is the mechanism by which terminals retrieve synaptic vesicles after exocytosis. Depending on the temporal demands placed on synapses during high-frequency synaptic transmission, synapses may use two alternative modes of synaptic vesicle retrieval, the conventional slow endosomal recycling or a faster rapid retrieval at the active zone, referred to as "kiss-and-run." By modulating Ca2+ microdomains associated with voltage-gated Ca2+ channels at active zones, NTs may elicit a switch from the slow to the fast mode of endocytosis of vesicles at presynaptic terminals during high-frequency synaptic transmission, allowing more reliable information transfer and neuronal signaling in the central nervous system.

摘要

神经营养因子(NTs)最近被证明对中枢和外周神经系统突触处的量子神经递质释放有显著影响。由于其活性依赖释放,以及蛋白质和受体的亚细胞定位,NTs非常适合通过在突触前终末的直接作用“微调”突触活性来改变神经元连接的强度。在此,作者以脑源性神经营养因子(BDNF)作为典型例子,提供了最新证据,证明NTs通过突触前机制增强突触处的量子神经递质释放。作者进一步提出,NTs在突触前终末作用的一个潜在靶点是终末在胞吐作用后回收突触小泡的机制。根据高频突触传递期间对突触的时间要求,突触可能使用两种替代的突触小泡回收模式,即传统的缓慢内体循环或在活性区更快的快速回收,即“亲吻-逃离”。通过调节与活性区电压门控Ca2+通道相关的Ca2+微区,NTs可能在高频突触传递期间引发突触前终末小泡内吞作用从缓慢模式向快速模式的转变,从而在中枢神经系统中实现更可靠的信息传递和神经元信号传导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdc4/2810653/0ecaf9959a79/nihms166553f1.jpg

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