4.6 Article

Pancreatic acinar cells: Molecular insight from studies of signal-transduction using transgenic animals

期刊

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.biocel.2010.07.007

关键词

Pancreatic acinar cell; Ca2+ signaling; Exocytosis; Inositol 1,4,5-trisphosphate receptor

资金

  1. National Institutes of Health [RO1-DK05458, R01-DE014756]

向作者/读者索取更多资源

Pancreatic acinar cells are classical exocrine gland cells. The apical regions of clusters of coupled acinar cells collectively form a lumen which constitutes the blind end of a tube created by ductal cells - a structure reminiscent of a bunch of grapes. When activated by neural or hormonal secretagogues, pancreatic acinar cells are stimulated to secrete a variety of proteins. These proteins are predominately inactive digestive enzyme precursors called zymogens. Acinar cell secretion is absolutely dependent on secretagogue-induced increases in intracellular free Ca2+. The increase in [Ca2+](i) has precise temporal and spatial characteristics as a result of the exquisite regulation of the proteins responsible for Ca2+ release, Ca2+ influx and Ca2+ clearance in the acinar cell. This brief review discusses recent studies in which transgenic animal models have been utilized to define in molecular detail the components of the Ca2+ signaling machinery which contribute to these characteristics. (C) 2010 Elsevier Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据