Lieu Zi Zhao, Derby Merran C, Teasdale Rohan D, Hart Charles, Gunn Priscilla, Gleeson Paul A
The Department of Biochemistry and Molecular Biology and Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Melbourne, Victoria 3010, Australia.
Mol Biol Cell. 2007 Dec;18(12):4979-91. doi: 10.1091/mbc.e07-06-0622. Epub 2007 Oct 3.
Retrograde transport pathways from early/recycling endosomes to the trans-Golgi network (TGN) are poorly defined. We have investigated the role of TGN golgins in retrograde trafficking. Of the four TGN golgins, p230/golgin-245, golgin-97, GCC185, and GCC88, we show that GCC88 defines a retrograde transport pathway from early endosomes to the TGN. Depletion of GCC88 in HeLa cells by interference RNA resulted in a block in plasma membrane-TGN recycling of two cargo proteins, TGN38 and a CD8 mannose-6-phosphate receptor cytoplasmic tail fusion protein. In GCC88-depleted cells, cargo recycling was blocked in the early endosome. Depletion of GCC88 dramatically altered the TGN localization of the t-SNARE syntaxin 6, a syntaxin required for endosome to TGN transport. Furthermore, the transport block in GCC88-depleted cells was rescued by syntaxin 6 overexpression. Internalized Shiga toxin was efficiently transported from endosomes to the Golgi of GCC88-depleted cells, indicating that Shiga toxin and TGN38 are internalized by distinct retrograde transport pathways. These findings have identified an essential role for GCC88 in the localization of TGN fusion machinery for transport from early endosomes to the TGN, and they have allowed the identification of a retrograde pathway which differentially selects TGN38 and mannose-6-phosphate receptor from Shiga toxin.
从早期/再循环内体到反式高尔基体网络(TGN)的逆行运输途径目前尚不清楚。我们研究了TGN高尔基体蛋白在逆行运输中的作用。在四种TGN高尔基体蛋白p230/高尔基体蛋白-245、高尔基体蛋白-97、GCC185和GCC88中,我们发现GCC88定义了一条从早期内体到TGN的逆行运输途径。通过干扰RNA使HeLa细胞中的GCC88缺失,导致两种货物蛋白(TGN38和一种CD8甘露糖-6-磷酸受体细胞质尾融合蛋白)的质膜-TGN再循环受阻。在GCC88缺失的细胞中,货物再循环在早期内体中被阻断。GCC88的缺失显著改变了t-SNARE syntaxin 6(一种内体到TGN运输所需的 syntaxin)在TGN的定位。此外,过表达syntaxin 6可挽救GCC88缺失细胞中的运输阻断。内化的志贺毒素能有效地从内体运输到GCC88缺失细胞的高尔基体,这表明志贺毒素和TGN38通过不同的逆行运输途径内化。这些发现确定了GCC88在将TGN融合机制定位以从早期内体运输到TGN中的重要作用,并且使我们能够鉴定出一条从志贺毒素中差异选择TGN38和甘露糖-6-磷酸受体的逆行途径。