Shen Dan-Na, Zhang Li-Hui, Wei Er-Qing, Yang Yi
Department of Pharmacology, Hangzhou Key Laboratory of Medical Neurobiology, School of Medicine, Hangzhou Normal University, Hangzhou, 310036, China.
Neurosci Bull. 2015 Aug;31(4):416-26. doi: 10.1007/s12264-015-1536-6. Epub 2015 Jul 2.
In the nervous system, neurons contact each other to form neuronal circuits and drive behavior, relying heavily on synaptic connections. The proper development and growth of synapses allows functional transmission of electrical information between neurons or between neurons and muscle fibers. Defects in synapse-formation or development lead to many diseases. Autophagy, a major determinant of protein turnover, is an essential process that takes place in developing synapses. During the induction of autophagy, proteins and cytoplasmic components are encapsulated in autophagosomes, which fuse with lysosomes to form autolysosomes. The cargoes are subsequently degraded and recycled. However, aberrant autophagic activity may lead to synaptic dysfunction, which is a common pathological characteristic in several disorders. Here, we review the current understanding of autophagy in regulating synaptic development and function. In addition, autophagy-related synaptic dysfunction in human diseases is also summarized.
在神经系统中,神经元相互接触以形成神经回路并驱动行为,这在很大程度上依赖于突触连接。突触的正常发育和生长使得神经元之间或神经元与肌纤维之间能够进行电信息的功能性传递。突触形成或发育中的缺陷会导致许多疾病。自噬是蛋白质周转的主要决定因素,是在发育中的突触中发生的一个重要过程。在自噬诱导过程中,蛋白质和细胞质成分被包裹在自噬体中,自噬体与溶酶体融合形成自溶酶体。随后,货物被降解并循环利用。然而,异常的自噬活动可能导致突触功能障碍,这是几种疾病中常见的病理特征。在这里,我们综述了目前对自噬在调节突触发育和功能方面的理解。此外,还总结了人类疾病中与自噬相关的突触功能障碍。