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仓鼠回肠钠依赖性胆汁酸转运蛋白的表达克隆与特性分析

Expression cloning and characterization of the hamster ileal sodium-dependent bile acid transporter.

作者信息

Wong M H, Oelkers P, Craddock A L, Dawson P A

机构信息

Department of Internal Medicine, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, North Carolina 27157.

出版信息

J Biol Chem. 1994 Jan 14;269(2):1340-7.

PMID:8288599
Abstract

Active uptake of bile acids from the lumen of the small intestine is mediated by an ileal Na(+)-dependent bile acid transport system. To identify components of this transport system, an expression cloning strategy was employed to isolate a hamster ileal cDNA that exhibits bile acid transport activity. By Northern blot analysis, mRNA for the cloned transporter was readily detected in ileum and kidney but was absent from liver and proximal small intestine. The transporter cDNA encoded a 348-amino acid protein with seven potential transmembrane domains and three possible N-linked glycosylation sites. The amino acid sequence was 35% identical and 63% similar to the rat liver Na+/bile acid cotransporter. After transfection into COS cells, the hamster cDNA transported taurocholate in a strict Na(+)-dependent fashion with an apparent Km of 33 microM. This taurocholate transport was inhibited by various bile acids but not by taurine or other organic anions. The Na+ dependence, saturability, and bile acid specificity of transport as well as the tissue specificity of mRNA expression strongly argue that the transporter cDNA characterized in this study is the Na+/bile acid cotransporter described previously in ileum.

摘要

小肠肠腔中胆汁酸的主动摄取是由回肠钠离子依赖性胆汁酸转运系统介导的。为了鉴定该转运系统的组成成分,采用表达克隆策略分离出一种具有胆汁酸转运活性的仓鼠回肠cDNA。通过Northern印迹分析,在回肠和肾脏中很容易检测到克隆转运体的mRNA,但在肝脏和近端小肠中则没有。该转运体cDNA编码一个348个氨基酸的蛋白质,具有七个潜在的跨膜结构域和三个可能的N-连接糖基化位点。其氨基酸序列与大鼠肝脏钠离子/胆汁酸共转运体的一致性为35%,相似性为63%。转染到COS细胞后,仓鼠cDNA以严格的钠离子依赖性方式转运牛磺胆酸盐,表观Km为33微摩尔。这种牛磺胆酸盐转运受到各种胆汁酸的抑制,但不受牛磺酸或其他有机阴离子的抑制。转运的钠离子依赖性、饱和性和胆汁酸特异性以及mRNA表达的组织特异性有力地表明,本研究中鉴定的转运体cDNA就是先前在回肠中描述的钠离子/胆汁酸共转运体。

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