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突触前钙信号传导的分子途径。

Molecular pathways for presynaptic calcium signaling.

作者信息

Augustine G J, Betz H, Bommert K, Charlton M P, DeBello W M, Hans M, Swandulla D

机构信息

Depatment of Neurobiology, Duke University, Durham, North Carolina 27710.

出版信息

Adv Second Messenger Phosphoprotein Res. 1994;29:139-54. doi: 10.1016/s1040-7952(06)80013-3.

Abstract

The results presented in this article describe two distinct, Ca-regulated molecular pathways in presynaptic terminals and implicate these two pathways in differentially mediating neurotransmitter secretion and PTP. Our current view of the Ca-dependent triggering of secretion and PTP is shown in Fig. 9. According to this scheme, differential activation of these two pathways is achieved by a combination of diffusion-based dilution of Ca that enters the terminal through voltage-gated Ca channels and by coupling these pathways to Ca receptors with different affinities for Ca ions. A simple way to achieve these conditions is to position these two receptors at different distances from the Ca channels, as shown in Fig. 2. Given that Ca ions are involved in activating many different presynaptic processes (Fig. 1), we propose that closer scrutiny of the molecular physiology of nerve terminals will reveal a wide variety of Ca-activated pathways responsible for producing these diverse processes.

摘要

本文所展示的结果描述了突触前终末中两种不同的、受钙调节的分子途径,并表明这两种途径在差异性介导神经递质分泌和强直后增强中发挥作用。我们目前关于钙依赖性分泌触发和强直后增强的观点如图9所示。根据该方案,这两种途径的差异性激活是通过以下两种方式实现的:一是通过电压门控钙通道进入终末的钙基于扩散的稀释作用,二是通过将这些途径与对钙离子具有不同亲和力的钙受体偶联。实现这些条件的一种简单方法是将这两种受体置于距钙通道不同的距离处,如图2所示。鉴于钙离子参与激活许多不同的突触前过程(图1),我们提出,对神经终末分子生理学进行更深入的研究将揭示出负责产生这些不同过程的多种钙激活途径。

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