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突触小泡循环与内溶酶体系统:形式与功能的重新评估

Synaptic Vesicle Recycling and the Endolysosomal System: A Reappraisal of Form and Function.

作者信息

Ivanova Daniela, Cousin Michael A

机构信息

Centre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.

Muir Maxwell Epilepsy Centre, University of Edinburgh, Edinburgh, United Kingdom.

出版信息

Front Synaptic Neurosci. 2022 Feb 25;14:826098. doi: 10.3389/fnsyn.2022.826098. eCollection 2022.

Abstract

The endolysosomal system is present in all cell types. Within these cells, it performs a series of essential roles, such as trafficking and sorting of membrane cargo, intracellular signaling, control of metabolism and degradation. A specific compartment within central neurons, called the presynapse, mediates inter-neuronal communication via the fusion of neurotransmitter-containing synaptic vesicles (SVs). The localized recycling of SVs and their organization into functional pools is widely assumed to be a discrete mechanism, that only intersects with the endolysosomal system at specific points. However, evidence is emerging that molecules essential for endolysosomal function also have key roles within the SV life cycle, suggesting that they form a continuum rather than being isolated processes. In this review, we summarize the evidence for key endolysosomal molecules in SV recycling and propose an alternative model for membrane trafficking at the presynapse. This includes the hypotheses that endolysosomal intermediates represent specific functional SV pools, that sorting of cargo to SVs is mediated via the endolysosomal system and that manipulation of this process can result in both plastic changes to neurotransmitter release and pathophysiology via neurodegeneration.

摘要

内溶酶体系统存在于所有细胞类型中。在这些细胞内,它发挥着一系列重要作用,如膜性货物的运输与分选、细胞内信号传导、代谢控制及降解。中枢神经元内一个名为突触前膜的特定区室,通过含神经递质的突触小泡(SVs)融合介导神经元间通讯。广泛认为,SVs的局部循环及其组织成功能池是一种离散机制,仅在特定点与内溶酶体系统相交。然而,越来越多的证据表明,内溶酶体功能所必需的分子在SV生命周期中也起着关键作用,这表明它们形成一个连续统一体,而非孤立过程。在本综述中,我们总结了内溶酶体关键分子在SV循环中的证据,并提出了突触前膜处膜运输的另一种模型。这包括以下假设:内溶酶体中间体代表特定的功能性SV池,货物向SVs的分选是通过内溶酶体系统介导的,以及对这一过程的操纵可导致神经递质释放的可塑性变化和通过神经退行性变引起的病理生理学改变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93dd/8916035/409c4a8a2065/fnsyn-14-826098-g001.jpg

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