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Journal of Lipid Research, Vol. 50, 2340-2357, December 2009
Bile acid transporters
Department of Internal Medicine and Department of Pathology, Wake Forest University School of Medicine, Winston-Salem, NC 27157
1 To whom correspondence should be addressed. e-mail: pdawson{at}wfubmc.edu
In liver and intestine, transporters play a critical role in maintaining the enterohepatic circulation and bile acid homeostasis. Over the past two decades, there has been significant progress toward identifying the individual membrane transporters and unraveling their complex regulation. In the liver, bile acids are efficiently transported across the sinusoidal membrane by the Na+ taurocholate cotransporting polypeptide with assistance by members of the organic anion transporting polypeptide family. The bile acids are then secreted in an ATP-dependent fashion across the canalicular membrane by the bile salt export pump. Following their movement with bile into the lumen of the small intestine, bile acids are almost quantitatively reclaimed in the ileum by the apical sodium-dependent bile acid transporter. The bile acids are shuttled across the enterocyte to the basolateral membrane and effluxed into the portal circulation by the recently indentified heteromeric organic solute transporter, OST
Supplementary key words bile acids cholesterol nuclear receptors cholestasis enterohepatic circulation Abbreviations: ASBT, apical sodium-dependent bile acid transporter; BRIC, benign recurrent intrahepatic cholestasis; BSEP, bile salt export pump; FXR, farnesoid X receptor; HNF, hepatocyte nuclear factor; IL, interleukin; JNK, Jun N-terminal kinase; LPS, lipopolysaccharide; LRH, liver receptor homolog; MRP, multidrug resistance protein; NTCP, Na+ taurocholate cotransporting polypeptide; OATP, organic anion transporting polypeptide; OST, organic solute transporter; PFIC, progressive familial intrahepatic cholestasis; RAR/RXR, retinoic acid receptor/retinoid X receptor; SHP, small heterodimer partner; TNF
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