Mechanisms and functional features of polarized membrane traffic in epithelial and hepatic cells
Open Access
- 1 December 1998
- journal article
- review article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 336 (2) , 257-269
- https://doi.org/10.1042/bj3360257
Abstract
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.Keywords
This publication has 92 references indexed in Scilit:
- Receptor and protein kinase C-mediated regulation of ARF binding to the Golgi complexNature, 1993
- Trafficking of glycosphingolipids in eukaryotic cells; sorting and recycling of lipidsBiochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1992
- Lipid flow in bile formationBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1992
- Caveolin, a protein component of caveolae membrane coatsPublished by Elsevier ,1992
- Control of exocytosis in adrenal chromaffin cellsBiochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1991
- Glycolipid transfer protein and intracellular traffic of glucosylceramideCellular and Molecular Life Sciences, 1990
- Glycerophospholipids and cholesterol composition of bile in bile-fistula rats treated with monensinBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1990
- Protein kinase C agonists inhibit bile secretion independently of effects on the microcirculation in the isolated perfused rat liverHepatology, 1989
- Ethinylestradiol administration selectively alters liver sinusoidal membrane lipid fluidity and protein compositionBiochemistry, 1988
- Transport of cholesterol from the endoplasmic reticulum to the plasma membrane.The Journal of cell biology, 1985