Autophagy in axonal and presynaptic development

被引:18
作者
Crawley, Oliver [1 ]
Grill, Brock [2 ,3 ,4 ]
机构
[1] Inst Neurociencias CSIC UMH, Unidad Neurobiol Celular & Sistemas, Alacant 03550, Spain
[2] Seattle Childrens Res Inst, Ctr Integrat Brain Res, Seattle, WA 98199 USA
[3] Univ Washington, Sch Med, Dept Pediat, Seattle, WA 98195 USA
[4] Univ Washington, Sch Med, Dept Pharmacol, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
GROWTH CONE; BIOLOGICAL FUNCTIONS; KINASE UNC-51; TRANSPORT; NEURODEGENERATION; COMPARTMENT; MECHANISMS; INHIBITION; HIGHWIRE; DISEASE;
D O I
10.1016/j.conb.2021.03.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The study of autophagy in the nervous system has predominantly centered on degeneration. Evidence is now cementing crucial roles for autophagy in neuronal development and growth, especially in axonal and presynaptic compartments. A picture is emerging that autophagy typically promotes the growth of axons and reduces presynaptic stability. Nonetheless, these are not rigid principles, and it remains unclear why autophagy does not always display these relationships during axonal and presynaptic development. Recent progress has identified mechanisms underlying spatiotemporal control of autophagy in neurons and begun to unravel how autophagy is integrated with other cellular processes, such as proteasomal degradation and axon guidance. Ultimately, understanding how autophagy is regulated and its role in the developing nervous system is key to comprehending how the nervous system assembles its stereotyped yet plastic configuration. It is also likely to inform how we think about neurodevelopmental disorders and neurodegenerative diseases.
引用
收藏
页码:139 / 148
页数:10
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