Strong activation of bile acid-sensitive ion channel (BASIC) by ursodeoxycholic acid

被引:24
|
作者
Wiemuth, Dominik [1 ]
Sahin, Hacer [2 ]
Lefevre, Catherine M. T. [1 ]
Wasmuth, Hermann E. [2 ]
Gruender, Stefan [1 ]
机构
[1] Rhein Westfal TH Aachen, Dept Physiol, Aachen, Germany
[2] Rhein Westfal TH Aachen, Dept Med 3, Aachen, Germany
关键词
acid-sensing ion channel; ASIC; BASIC; bile acid; BLINaC; cholangiocyte; DEG/ENaC; ENaC; epithelial Na+ channel; NA+ CHANNEL; TAUROURSODEOXYCHOLIC ACID; FUNCTIONAL EXPRESSION; KNOCKOUT MICE; LIVER; INTESTINE; CLONING; DIARYLAMIDINES; INHIBITION; MECHANISMS;
D O I
10.4161/chan.22406
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bile acid-sensitive ion channel (BASIC) is a member of the DEG/ENaC gene family of unknown function. Rat BASIC (rBASIC) is inactive at rest. We have recently shown that cholangiocytes, the epithelial cells lining the bile ducts, are the main site of BASIC expression in the liver and identified bile acids, in particular hyo- and chenodeoxycholic acid, as agonists of rBASIC. Moreover, it seems that extracellular divalent cations stabilize the resting state of rBASIC, because removal of extracellular divalent cations opens the channel. In this addendum, we demonstrate that removal of extracellular divalent cations potentiates the activation of rBASIC by bile acids, suggesting an allosteric mechanism. Furthermore, we show that rBASIC is strongly activated by the anticholestatic bile acid ursodeoxycholic acid (UDCA), suggesting that BASIC might mediate part of the therapeutic effects of UDCA.
引用
收藏
页码:38 / 42
页数:5
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