Acta Gastroenterol Belg 1996 Jan 01;592:159-62.

Mechanisms of hepatic transport and bile secretion.

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The transport processes responsible for bile flow are reviewed. Canalicular bile acid-dependent flow is the result of active transport of bile acids by the hepatocyte into bile canaliculi. Bile acids are taken up by at least two transport systems whose mRNAs have been expressed in Xenopus oocytes: a Na(+)-dependent system, named NTCP, and a Na(+)-independent system, named OATP. Bile acids are then secreted into bile by two other transport systems, an ATP-dependent system and an "electrogenic" voltage-dependent system. It is not known whether these two systems are mediated by the same protein or by two different proteins. Canalicular bile acid-independent flow is mainly the result of the secretion of glutathione into bile. The canalicular membrane contains also several proteins of the MDR (Multi Drug Resistance) family. MDR1 is responsible for biliary secretion of cationic drugs. MDR2 plays a major role in the secretion of phospholipids. A third MDR related protein has been shown recently to be the canalicular carrier of organic anions, like bilirubin and dyes (the canalicular Multiple Organic Anion Transporter, or cMOAT). Biliary epithelial cells secrete a bicarbonate rich solution, mostly in response to secretion. This secretion depends on the presence on the apical membrane of these cells of the CFTR, a chloride channel activated by cAMP, and of a chloride/bicarbonate exchanger. Knowledge of these transport systems should allow a better understanding of the mechanisms involved in cholestasis.

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Species referenced: Xenopus
Genes referenced: abcb1 abcc2 camp cftr slc10a1 slco1a2