Institut Pasteur, Unité de Traffic Membranaire et Pathogenèse, 75015 Paris, France.
Mol Biol Cell. 2011 Dec;22(23):4621-34. doi: 10.1091/mbc.E11-04-0320. Epub 2011 Oct 12.
Sorting of glycosylphosphatidyl-inositol--anchored proteins (GPI-APs) in polarized epithelial cells is not fully understood. Oligomerization in the Golgi complex has emerged as the crucial event driving apical segregation of GPI-APs in two different kind of epithelial cells, Madin-Darby canine kidney (MDCK) and Fisher rat thyroid (FRT) cells, but whether the mechanism is conserved is unknown. In MDCK cells cholesterol promotes GPI-AP oligomerization, as well as apical sorting of GPI-APs. Here we show that FRT cells lack this cholesterol-driven oligomerization as apical sorting mechanism. In these cells both apical and basolateral GPI-APs display restricted diffusion in the Golgi likely due to a cholesterol-enriched membrane environment. It is striking that N-glycosylation is the critical event for oligomerization and apical sorting of GPI-APs in FRT cells but not in MDCK cells. Our data indicate that at least two mechanisms exist to determine oligomerization in the Golgi leading to apical sorting of GPI-APs. One depends on cholesterol, and the other depends on N-glycosylation and is insensitive to cholesterol addition or depletion.
糖基磷脂酰肌醇锚定蛋白(GPI-APs)在极化上皮细胞中的分拣过程尚未完全阐明。寡聚化在高尔基复合体中被认为是驱动两种不同的上皮细胞(Madin-Darby 犬肾(MDCK)和Fisher 大鼠甲状腺(FRT)细胞)中 GPI-AP 顶端分离的关键事件,但该机制是否保守尚不清楚。在 MDCK 细胞中,胆固醇促进 GPI-AP 寡聚化以及 GPI-AP 的顶端分拣。在这里,我们表明 FRT 细胞缺乏这种胆固醇驱动的寡聚化作为顶端分拣机制。在这些细胞中,顶端和基底外侧的 GPI-AP 在高尔基体内显示出受限的扩散,这可能是由于富含胆固醇的膜环境。引人注目的是,N-糖基化是 FRT 细胞中 GPI-AP 寡聚化和顶端分拣的关键事件,但在 MDCK 细胞中并非如此。我们的数据表明,至少存在两种机制来确定高尔基体内的寡聚化,从而导致 GPI-AP 的顶端分拣。一种依赖于胆固醇,另一种依赖于 N-糖基化,并且对胆固醇的添加或耗尽不敏感。