SNAREs are concentrated in cholesterol-dependent clusters that define docking and fusion sites for exocytosis

被引:532
作者
Lang, T
Bruns, D
Wenzel, D
Riedel, D
Holroyd, P
Thiele, C
Jahn, R [1 ]
机构
[1] Max Planck Inst Biophys Chem, Dept Neurobiol, D-37077 Gottingen, Germany
[2] Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany
关键词
cholesterol; exocytosis; PC12; cells; SNAREs;
D O I
10.1093/emboj/20.9.2202
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During exocytosis, SNARE vesicles interact with the corresponding SNARE proteins in the plasmalemma to initiate the fusion reaction. However, it is unknown whether SNAREs are uniformly distributed in the membrane or whether specialized fusion sites exist. Here we report that in the plasmalemma, syntaxins are concentrated in 200 nm large, cholesterol-dependent clusters at which secretory vesicles preferentially dock and fuse. The syntaxin clusters are distinct from cholesterol-dependent membrane rafts since they are Triton X-100-soluble and do not co-patch with raft markers. Synaptosomal-associated protein (SNAP)-25 is also clustered in spots, which partially overlap with syntaxin. Cholesterol depletion causes dispersion of these clusters, which is associated with a strong reduction in the rate of secretion, whereas the characteristics of individual exocytic events are unchanged. This suggests that high local concentrations of SNAREs are required for efficient fusion.
引用
收藏
页码:2202 / 2213
页数:12
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