Zegers M M, Hoekstra D
Department of Physiological Chemistry, University of Groningen, A. Deusinglaan 1, 9713 EV Groningen, The Netherlands.
Biochem J. 1998 Dec 1;336 ( Pt 2)(Pt 2):257-69. doi: 10.1042/bj3360257.
Epithelial cells express plasma-membrane polarity in order to meet functional requirements that are imposed by their interaction with different extracellular environments. Thus apical and basolateral membrane domains are distinguished that are separated by tight junctions in order to maintain the specific lipid and protein composition of each domain. In hepatic cells, the plasma membrane is also polarized, containing a sinusoidal (basolateral) and a bile canalicular (apical)-membrane domain. Relevant to the biogenesis of these domains are issues concerning sorting, (co-)transport and regulation of transport of domain-specific membrane components. In epithelial cells, specific proteins and lipids, destined for the apical membrane, are sorted in the trans-Golgi network (TGN), which involves their sequestration into cholesterol/sphingolipid 'rafts', followed by 'direct' transport to the apical membrane. In hepatic cells, a direct apical transport pathway also exists, as revealed by transport of sphingolipids from TGN to the apical membrane. This is remarkable, since in these cells numerous apical membrane proteins are 'indirectly' sorted, i.e. they are first transferred to the basolateral membrane prior to their subsequent transcytosis to the apical membrane. This raises intriguing questions as to the existence of specific lipid rafts in hepatocytes. As demonstrated in studies with HepG2 cells, it has become evident that, in hepatic cells, apical transport pathways can be regulated by protein kinase activity, which in turn modulates cell polarity. Finally, an important physiological function of hepatic cells is their involvement in intracellular transport and secretion of bile-specific lipids. Mechanisms of these transport processes, including the role of multidrug-resistant proteins in lipid translocation, will be discussed in the context of intracellular vesicular transport. Taken together, hepatic cell systems provide an important asset to studies aimed at elucidating mechanisms of sorting and trafficking of lipids (and proteins) in polarized cells in general.
上皮细胞表达质膜极性,以满足其与不同细胞外环境相互作用所带来的功能需求。因此,顶端和基底外侧膜结构域得以区分,它们由紧密连接分隔开,以维持每个结构域特定的脂质和蛋白质组成。在肝细胞中,质膜也呈极化状态,包含窦状(基底外侧)和胆小管(顶端)膜结构域。与这些结构域的生物发生相关的问题包括特定膜成分的分选、(共)运输以及运输调节。在上皮细胞中, destined for the apical membrane的特定蛋白质和脂质在反式高尔基体网络(TGN)中进行分选,这涉及将它们隔离到胆固醇/鞘脂“筏”中,随后“直接”运输到顶端膜。在肝细胞中,也存在一条直接的顶端运输途径,鞘脂从TGN运输到顶端膜就揭示了这一点。这很值得注意,因为在这些细胞中,许多顶端膜蛋白是“间接”分选的,即它们首先被转移到基底外侧膜,然后再通过转胞吞作用运输到顶端膜。这就引发了关于肝细胞中是否存在特定脂质筏的有趣问题。正如在对HepG2细胞的研究中所表明的,很明显,在肝细胞中,顶端运输途径可由蛋白激酶活性调节,而蛋白激酶活性又反过来调节细胞极性。最后,肝细胞的一项重要生理功能是它们参与胆汁特异性脂质的细胞内运输和分泌。这些运输过程的机制,包括多药耐药蛋白在脂质转运中的作用,将在细胞内囊泡运输的背景下进行讨论。总之,肝细胞系统为旨在阐明一般极化细胞中脂质(和蛋白质)分选和运输机制的研究提供了重要资源。