Calcium signaling and the secretory activity of bile duct epithelia

被引:17
作者
Amaya, Maria Jimena [1 ]
Nathanson, Michael H. [1 ]
机构
[1] Yale Univ, Sch Med, Sect Digest Dis, New Haven, CT 06520 USA
关键词
Calcium; InsP3; receptors; Cholangiocytes; Secretion; INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR; PANCREATIC ACINAR-CELLS; III INSP(3) RECEPTOR; ADENOSINE-TRIPHOSPHATE RELEASE; HEPATOCYTE GAP-JUNCTIONS; ISOLATED RAT HEPATOCYTES; TAUROURSODEOXYCHOLIC ACID; BICARBONATE SECRETION; PURINERGIC REGULATION; BILIARY EPITHELIUM;
D O I
10.1016/j.ceca.2014.02.003
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Cytosolic calcium (Ca-i(2+)) is a second messenger that is important for the regulation of secretion in many types of tissues. Bile duct epithelial cells, or cholangiocytes, are polarized epithelia that line the biliary tree in liver and are responsible for secretion of bicarbonate and other solutes into bile. Ca-i(2+) signaling plays an important role in the regulation of secretion by cholangiocytes, and this review discusses the machinery involved in the formation of Ca2+ signals in cholangiocytes, along with the evidence that these signals regulate ductular secretion. Finally, this review discusses the evidence that impairments in cholangiocyte Ca2+ signaling play a primary role in the pathogenesis of cholestatic disorders, in which hepatic bile secretion is impaired. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:317 / 324
页数:8
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