Early/recycling endosomes-to-TGN transport involves two SNARE complexes and a Rab6 isoform

被引:433
作者
Mallard, F
Tang, BL
Galli, T
Tenza, D
Saint-Pol, A
Yue, X
Antony, C
Hong, WJ
Goud, B
Johannes, L
机构
[1] Inst Curie, CNRS, UMR144, Traff & Signaling Lab, F-75248 Paris 05, France
[2] Inst Curie, INSERM, U536, F-75248 Paris 05, France
[3] Inst Mol & Cell Biol, Membrane Biol Lab, Singapore 117609, Singapore
关键词
shiga toxin; early/recycling endosomes; SNARE; Rab protein; retrograde transport;
D O I
10.1083/jcb.200110081
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The molecular mechanisms underlying early/recycling endosomes-to-TGN transport are still not understood. We identified interactions between the TGN-localized putative t-SNARES syntaxin 6, syntaxin 16, and Vti1a, and two early/recycling endosomal v-SNARES, VAMP3/cellubrevin, and VAMP4. Using a novel permeabilized cell system, these proteins were functionally implicated in the post-Golgi retrograde transport step. The function of Rab6a' was also required, whereas its closely related isoform, Rab6a, has previously been implicated in Golgi-to-endoplasmic reticulum transport. Thus, our study shows that membrane exchange between the early endocytic and the biosynthetic/secretory pathways involves specific components of the Rab and SNARE machinery, and suggests that retrograde transport between early/recycling endosomes and the endoplasmic reticulum is critically dependent on the sequential action of two members of the Rab6 subfamily.
引用
收藏
页码:653 / 664
页数:12
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