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脊椎动物突触前活性区装配:多种分子和细胞机制的作用。

Vertebrate Presynaptic Active Zone Assembly: a Role Accomplished by Diverse Molecular and Cellular Mechanisms.

机构信息

Centro de Envejecimiento y Regeneración (CARE), Departamento de Biología Celular y Molecular, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.

Center for Healthy Brain Ageing, School of Psychiatry, Faculty of Medicine, University of New South Wales, Sydney, Australia.

出版信息

Mol Neurobiol. 2018 Jun;55(6):4513-4528. doi: 10.1007/s12035-017-0661-9. Epub 2017 Jul 6.

Abstract

Among all the biological systems in vertebrates, the central nervous system (CNS) is the most complex, and its function depends on specialized contacts among neurons called synapses. The assembly and organization of synapses must be exquisitely regulated for a normal brain function and network activity. There has been a tremendous effort in recent decades to understand the molecular and cellular mechanisms participating in the formation of new synapses and their organization, maintenance, and regulation. At the vertebrate presynapses, proteins such as Piccolo, Bassoon, RIM, RIM-BPs, CAST/ELKS, liprin-α, and Munc13 are constant residents and participate in multiple and dynamic interactions with other regulatory proteins, which define network activity and normal brain function. Here, we review the function of these active zone (AZ) proteins and diverse factors involved in AZ assembly and maintenance, with an emphasis on axonal trafficking of precursor vesicles, protein homo- and hetero-oligomeric interactions as a mechanism of AZ trapping and stabilization, and the role of F-actin in presynaptic assembly and its modulation by Wnt signaling.

摘要

在脊椎动物的所有生物系统中,中枢神经系统(CNS)是最复杂的,其功能取决于神经元之间称为突触的特殊接触。突触的组装和组织必须受到精细的调节,以维持正常的大脑功能和网络活动。近几十年来,人们一直在努力理解参与新突触形成及其组织、维持和调节的分子和细胞机制。在脊椎动物的突触前, Piccolo、Bassoon、RIM、RIM-BPs、CAST/ELKS、liprin-α 和 Munc13 等蛋白是固定居民,并与其他调节蛋白进行多种动态相互作用,这些相互作用定义了网络活动和正常的大脑功能。在这里,我们回顾了这些活性区(AZ)蛋白的功能以及参与 AZ 组装和维持的多种因素,重点介绍了前导囊泡的轴突运输、蛋白同型和异型寡聚相互作用作为 AZ 捕获和稳定的机制,以及 F-肌动蛋白在突触前组装中的作用及其受 Wnt 信号的调节。

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