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FM1-43 的光转化揭示了单个突触中突触囊泡再循环和对肌动蛋白动力学药理学干扰敏感性的差异。

Photoconversion of FM1-43 Reveals Differences in Synaptic Vesicle Recycling and Sensitivity to Pharmacological Disruption of Actin Dynamics in Individual Synapses.

机构信息

Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC) , Madrid 28040 , Spain.

出版信息

ACS Chem Neurosci. 2019 Apr 17;10(4):2045-2059. doi: 10.1021/acschemneuro.8b00712. Epub 2019 Feb 27.

Abstract

The cycling of synaptic vesicles ensures that neurons can communicate adequately through their synapses on repeated occasions when activity is sustained, and several steps in this cycle are modulated by actin. The effects of pharmacological stabilization of actin with jasplakinolide or its depolymerization with latrunculin A was assessed on the synaptic vesicle cycle at individual boutons of cerebellar granule cells, using FM1-43 imaging to track vesicle recycling and its photoconversion to specifically label recycled organelles. Remarkable differences in the recycling capacity of individual boutons are evident, and their dependence on the actin cytoskeleton for recycling is clear. Disrupting actin dynamics causes a loss of functional boutons, and while this indicates that exo/endocytotic cycling in boutons is fully dependent on such events, this dependence is only partial in other boutons. Indeed, exocytosis and vesicle trafficking are impaired significantly by stabilizing or depolymerizing actin, whereas repositioning recycled vesicles at the active zone seems to be dependent on actin polymerization alone. These findings support the hypothesis that different steps of synaptic vesicle cycling depend on actin dynamics and that such dependence varies among individual boutons.

摘要

囊泡循环确保神经元在活动持续时能够通过其突触进行充分的通讯,并且该循环中的几个步骤受到肌动蛋白的调节。使用 FM1-43 成像来跟踪囊泡再循环及其光转化以专门标记再循环细胞器,评估用 Jasplakinolide 稳定肌动蛋白或用 Latrunculin A 解聚肌动蛋白对小脑颗粒细胞的单个突触及的囊泡循环的影响。个体突触及的再循环能力存在显著差异,并且它们的再循环依赖于肌动蛋白细胞骨架。破坏肌动蛋白动力学会导致功能突触及丧失,虽然这表明突触及中的胞吐/内吞循环完全依赖于这些事件,但在其他突触及中这种依赖性只是部分的。事实上,通过稳定或解聚肌动蛋白,胞吐作用和囊泡运输受到显著损害,而将再循环的囊泡重新定位到活性区似乎仅依赖于肌动蛋白聚合。这些发现支持这样的假设,即突触囊泡循环的不同步骤依赖于肌动蛋白动力学,并且这种依赖性在个体突触及之间存在差异。

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