...
首页> 外文期刊>Molecular Neurobiology >Activity-Dependent Bulk Synaptic Vesicle Endocytosis—A Fast, High Capacity Membrane Retrieval Mechanism
【24h】

Activity-Dependent Bulk Synaptic Vesicle Endocytosis—A Fast, High Capacity Membrane Retrieval Mechanism

机译:依赖活动的大突触囊泡内吞作用—一种快速,高容量的膜检索机制。

获取原文
获取原文并翻译 | 示例
           

摘要

Central nerve terminals are placed under considerable stress during intense stimulation due to large numbers of synaptic vesicles (SVs) fusing with the plasma membrane. Classical clathrin-dependent SV endocytosis cannot correct for the large increase in nerve terminal surface area in the short term, due to its slow kinetics and low capacity. During such intense stimulation, an additional SV retrieval pathway is recruited called bulk endocytosis. Recent studies have shown that bulk endocytosis fulfils all of the physiological requirements to remedy the acute changes in nerve terminal surface area to allow the nerve terminal to continue to function. This review will summarise the recent developments in the field that characterise the physiology of bulk endocytosis which show that it is a fast, activity-dependent and high capacity mechanism that is essential for the function of central nerve terminals.
机译:由于大量的突触小泡(SVs)与质膜融合,因此在强烈刺激期间,中枢神经末梢处于相当大的压力之下。由于其缓慢的动力学和低容量,经典的网格蛋白依赖性SV内吞作用不能在短期内纠正神经末梢表面积的大幅增加。在这种强烈刺激过程中,会募集另一种SV回收途径,称为大量内吞作用。最近的研究表明,大量内吞能满足所有生理要求,以纠正神经末梢表面积的急性变化,从而使神经末梢继续起作用。这篇综述将总结该领域内表征体细胞内吞作用生理学的最新进展,这表明它是一种快速,依赖于活性的高容量机制,对于中枢神经末梢的功能至关重要。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号