The role of ESCRT during development and functioning of the nervous system

被引:29
作者
Sadoul, Remy [1 ,2 ]
Laporte, Marine H. [1 ,2 ,3 ]
Chassefeyre, Romain [1 ,2 ,4 ]
Chi, Kwang Il [1 ,2 ]
Goldberg, Yves [1 ,2 ]
Chatellard, Christine [1 ,2 ]
Hemming, Fiona J. [1 ,2 ]
Fraboulet, Sandrine [1 ,2 ,5 ]
机构
[1] INSERM, U1216, F-38042 Grenoble, France
[2] Univ Grenoble Alpes, Inst Neurosci, F-38042 Grenoble, France
[3] Univ Geneva, Dept Cell Biol, CH-1211 Geneva 4, Switzerland
[4] Dept Mol & Expt Med, La Jolla, CA 92037 USA
[5] INSERM IAB, Unite 823, F-38000 Grenoble, France
关键词
ALIX; CHMP; Synapse; Cortex development; FRONTOTEMPORAL DEMENTIA; DENDRITIC SPINES; III COMPLEX; MULTIVESICULAR BODIES; ALIX; PROTEIN; CHMP2B; TRAFFICKING; APOPTOSIS; ENDOSOMES;
D O I
10.1016/j.semcdb.2017.08.013
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The endosomal sorting complex required for transport (ESCRT) is made of subcomplexes (ESCRT 0-III), crucial to membrane remodelling at endosomes, nuclear envelope and cell surface. ESCRT-III shapes membranes and in most cases cooperates with the ATPase VPS4 to mediate fission of membrane necks from the inside. The first ESCRT complexes mainly serve to catalyse the formation of ESCRT-III but can be bypassed by accessory proteins like the Alg-2 interacting protein-X (ALIX). In the nervous system, ALIX/ESCRT controls the survival of embryonic neural progenitors and later on the outgrowth and pruning of axons and dendrites, all necessary steps to establish a functional brain. In the adult brain, ESCRTs allow the endosomal turn over of synaptic vesicle proteins while stable ESCRT complexes might serve as scaffolds for the postsynaptic parts. The necessity of ESCRT for the harmonious function of the brain has its pathological counterpart, the mutations in CHMP2B of ESCRT-III giving rise to several neurodegenerative diseases. (c) 2017 Published by Elsevier Ltd.
引用
收藏
页码:40 / 49
页数:10
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