Ca2+ influx inhibits dynamin and arrests synaptic vesicle endocytosis at the active zone

被引:79
作者
Cousin, MA [1 ]
Robinson, PJ [1 ]
机构
[1] Childrens Med Res Inst, Cell Signaling Unit, Sydney, NSW 2145, Australia
关键词
endocytosis; exocytosis; FM2-10; dynamin; calcium; nerve terminal;
D O I
10.1523/JNEUROSCI.20-03-00949.2000
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Ca2+ entry into nerve terminals through clusters of voltage-dependent Ca2+ channels (VDCCs) at active zones creates a microdomain of elevated intracellular free Ca2+ concentration ([Ca2+](i)) that stimulates exocytosis. We show that this VDCC-mediated [Ca2+](i) elevation has no specific role in stimulating endocytosis but can inhibit endocytosis evoked by three different methods in isolated mammalian nerve terminals. The inhibition can be relieved by using either VDCC antagonists or fast, but not slow, binding intracellular Ca2+ chelators. The Ca2+ dependent inhibition of endocytosis is mimicked in vitro by a low-affinity inhibition of dynamin I vesiculation of phospholipids. Increased [Ca2+](i) also inhibits dynamin II GTPase activity and receptor-mediated endocytosis in non-neuronal cells. VDCC-meditated Ca2+ entry inhibits dynamin-mediated endocytosis at the active zone and provides neurons with a mechanism to clear recycling vesicles to nonactive zone regions during periods of high activity.
引用
收藏
页码:949 / 957
页数:9
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