Utskarpen Audrun, Slagsvold Hege H, Dyve Anne Berit, Skånland Sigrid S, Sandvig Kirsten
Institute for Cancer Research, Centre for Cancer Biomedicine, The Norwegian Radium Hospital, Montebello, Oslo, Norway.
Biochem Biophys Res Commun. 2007 Jun 29;358(2):566-70. doi: 10.1016/j.bbrc.2007.04.159. Epub 2007 May 4.
The bacterial toxin Shiga toxin (Stx) is transported retrogradely from early endosomes to the Golgi apparatus on its way to the endoplasmic reticulum (ER) and the cytosol. In this study we explored the functions of the two phosphoinositide binding proteins Sorting nexin 1 (SNX1) and Sorting nexin 2 (SNX2) in endosomal sorting of the toxin. When Vero cells were depleted of either SNX1 or SNX2 by small interfering RNA (siRNA), Stx transport to the trans-Golgi network (TGN) was impaired by > or = 40%, whereas combined depletion of SNX1 and SNX2 gave a total inhibition of approximately 80%. Inhibition of PI(3)P formation by wortmannin resulted in a similar reduction. Thus, although being partly redundant, both SNX1 and SNX2 are required for efficient Stx trafficking to the Golgi apparatus.
细菌毒素志贺毒素(Stx)在其前往内质网(ER)和胞质溶胶的途中,从早期内体逆向转运至高尔基体。在本研究中,我们探究了两种磷酸肌醇结合蛋白分选连接蛋白1(SNX1)和分选连接蛋白2(SNX2)在内体毒素分选中的功能。当用小干扰RNA(siRNA)使Vero细胞中的SNX1或SNX2耗尽时,Stx向反式高尔基体网络(TGN)的转运受损>或= 40%,而SNX1和SNX2的联合耗尽导致约80%的完全抑制。渥曼青霉素对PI(3)P形成的抑制导致了类似程度的降低。因此,尽管部分冗余,但SNX1和SNX2都是Stx有效转运至高尔基体所必需的。