突触发生
生物
神经科学
中枢神经系统
神经胶质
胆固醇
载脂蛋白E
突触
平衡
细胞生物学
内分泌学
内科学
医学
疾病
作者
Daniela H. Mauch,Karl Nägler,Stefan Schumacher,Christian Göritz,Eva-Christina Müller,Albrecht Otto,Frank W. Pfrieger
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2001-11-09
卷期号:294 (5545): 1354-1357
被引量:1608
标识
DOI:10.1126/science.294.5545.1354
摘要
The molecular mechanisms controlling synaptogenesis in the central nervous system (CNS) are poorly understood. Previous reports showed that a glia-derived factor strongly promotes synapse development in cultures of purified CNS neurons. Here, we identify this factor as cholesterol complexed to apolipoprotein E–containing lipoproteins. CNS neurons produce enough cholesterol to survive and grow, but the formation of numerous mature synapses demands additional amounts that must be provided by glia. Thus, the availability of cholesterol appears to limit synapse development. This may explain the delayed onset of CNS synaptogenesis after glia differentiation and neurobehavioral manifestations of defects in cholesterol or lipoprotein homeostasis.
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