Recent advances in the molecular cloning of membrane transport systems that determine
bile formation have facilitated studies of the molecular mechanisms of cholestatic
liver disease. The present review summarizes what has been learned about the molecular
alterations of these membrane transporters in hepatocytes and cholangiocytes in acquired
cholestatic liver disorders. Much of this information has been obtained from the study
of animal models of cholestasis and from more limited studies in clinical cholestatic
liver diseases. Many of these responses may be interpreted as adaptations that serve
to diminish cholestatic liver injury.
cholestasis - membrane transporters - hepatocyte - cholangiocyte - export pumps