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肌动蛋白及其调节蛋白对突触结构和功能的控制。

Control of Synapse Structure and Function by Actin and Its Regulators.

机构信息

Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.

Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520, USA.

出版信息

Cells. 2022 Feb 9;11(4):603. doi: 10.3390/cells11040603.

Abstract

Neurons transmit and receive information at specialized junctions called synapses. Excitatory synapses form at the junction between a presynaptic axon terminal and a postsynaptic dendritic spine. Supporting the shape and function of these junctions is a complex network of actin filaments and its regulators. Advances in microscopic techniques have enabled studies of the organization of actin at synapses and its dynamic regulation. In addition to highlighting recent advances in the field, we will provide a brief historical perspective of the understanding of synaptic actin at the synapse. We will also highlight key neuronal functions regulated by actin, including organization of proteins in the pre- and post- synaptic compartments and endocytosis of ion channels. We review the evidence that synapses contain distinct actin pools that differ in their localization and dynamic behaviors and discuss key functions for these actin pools. Finally, whole exome sequencing of humans with neurodevelopmental and psychiatric disorders has identified synaptic actin regulators as key disease risk genes. We briefly summarize how genetic variants in these genes impact neurotransmission via their impact on synaptic actin.

摘要

神经元在称为突触的专门连接处传递和接收信息。兴奋性突触形成于突触前轴突末梢和突触后树突棘之间的连接处。支持这些连接处的形状和功能的是一个复杂的肌动蛋白丝网络及其调节剂。显微镜技术的进步使得研究突触处肌动蛋白的组织及其动态调节成为可能。除了强调该领域的最新进展外,我们还将简要回顾一下突触处肌动蛋白理解的历史。我们还将重点介绍受肌动蛋白调节的关键神经元功能,包括前突触和后突触隔室中蛋白质的组织和离子通道的内吞作用。我们回顾了证据表明突触包含不同的肌动蛋白池,这些池在其定位和动态行为上有所不同,并讨论了这些肌动蛋白池的关键功能。最后,对具有神经发育和精神疾病的人类的全外显子组测序已经确定了突触肌动蛋白调节剂是关键的疾病风险基因。我们简要总结了这些基因中的遗传变异如何通过影响突触肌动蛋白来影响神经传递。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9432/8869895/3101b8a55b25/cells-11-00603-g001.jpg

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