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缺乏环鸟苷酸依赖性蛋白激酶II的小鼠的肠道分泌缺陷和侏儒症

Intestinal secretory defects and dwarfism in mice lacking cGMP-dependent protein kinase II.

作者信息

Pfeifer A, Aszódi A, Seidler U, Ruth P, Hofmann F, Fässler R

机构信息

Institut f-ur Pharmakologie und Toxikologie, Technische Universität München, Biedersteiner Strasse 29, D-80802 M-unchen, Germany.

出版信息

Science. 1996 Dec 20;274(5295):2082-6. doi: 10.1126/science.274.5295.2082.

Abstract

Cyclic guanosine 3',5'-monophosphate (cGMP)-dependent protein kinases (cGKs) mediate cellular signaling induced by nitric oxide and cGMP. Mice deficient in the type II cGK were resistant to Escherichia coli STa, an enterotoxin that stimulates cGMP accumulation and intestinal fluid secretion. The cGKII-deficient mice also developed dwarfism that was caused by a severe defect in endochondral ossification at the growth plates. These results indicate that cGKII plays a central role in diverse physiological processes.

摘要

环磷酸鸟苷(cGMP)依赖性蛋白激酶(cGKs)介导一氧化氮和cGMP诱导的细胞信号传导。II型cGK缺陷的小鼠对大肠杆菌STa具有抗性,STa是一种能刺激cGMP积累和肠液分泌的肠毒素。cGKII缺陷的小鼠还出现了侏儒症,这是由生长板软骨内骨化的严重缺陷引起的。这些结果表明,cGKII在多种生理过程中起核心作用。

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