Hickinson D M, Lucocq J M, Towler M C, Clough S, James J, James S R, Downes C P, Ponnambalam S
Department of Biochemistry, Medical Sciences Institute, University of Dundee, Dundee DD1 4HN, UK.
Curr Biol. 1997 Dec 1;7(12):987-90. doi: 10.1016/s0960-9822(06)00418-0.
The eukaryotic trans-Golgi network (TGN) is a key site for the formation of transport vesicles destined for different intracellular compartments [1]. A key marker for the mammalian TGN is TGN38/46 [2]. This integral membrane glycoprotein cycles between the TGN and the cell surface and is implicated in recruitment of cytosolic factors and regulation of at least one type of vesicle formation at the mammalian TGN [2] [3]. In this study, we have identified a phosphatidylinositol (PtdIns)-specific 3-kinase activity associated with the human orthologue (TGN46), which is sensitive to lipid kinase inhibitors. Treatment of HeLa cells with low levels of these inhibitors reveals subtle morphological changes in TGN46-positive compartments. Our findings suggest a role for PtdIns 3-kinases and presumably for the product, PtdIns 3-phosphate (PtdIns3P), in the formation of secretory transport vesicles by mechanisms conserved in yeast and mammals.
真核生物反式高尔基体网络(TGN)是形成运往不同细胞内区室的运输小泡的关键位点[1]。哺乳动物TGN的一个关键标志物是TGN38/46[2]。这种整合膜糖蛋白在TGN和细胞表面之间循环,并且与胞质因子的募集以及哺乳动物TGN处至少一种小泡形成的调节有关[2][3]。在本研究中,我们鉴定出一种与人同源物(TGN46)相关的磷脂酰肌醇(PtdIns)特异性3-激酶活性,其对脂质激酶抑制剂敏感。用低水平的这些抑制剂处理HeLa细胞会揭示TGN46阳性区室中的细微形态变化。我们的研究结果表明,磷脂酰肌醇3-激酶以及推测其产物磷脂酰肌醇3-磷酸(PtdIns3P)通过酵母和哺乳动物中保守的机制在分泌性运输小泡的形成中发挥作用。