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生长激素释放因子对生长激素细胞中磷酸肌醇水解的影响。

Effect of growth hormone-releasing factor on phosphoinositide hydrolysis in somatotrophs.

作者信息

French M B, Lussier B T, Moor B C, Kraicer J

机构信息

Department of Physiology, University of Western Ontario, London, Canada.

出版信息

Mol Cell Endocrinol. 1990 Sep 10;72(3):221-6. doi: 10.1016/0303-7207(90)90146-y.

Abstract

We studied the role of the phosphatidylinositol system in the action of growth hormone-releasing factor (GRF). We asked whether GRF stimulates the activity of phospholipase C by determining GRF-induced changes in 32P labeling of the individual phosphoinositides and inositol phosphates in purified rat somatotrophs. The somatotrophs were challenged with GRF (10(-7)M) for 0.33, 1, 3, 10, 30, and 90 min. GRF did not significantly or consistently alter 32P incorporation into phosphatidylinositol bisphosphate (PIP2), phosphatidylinositol monophosphate (PIP), or phosphatidylinositol (PI), except for a small reduction in PIP labeling at 90 min. In general the level of 32P incorporation into the inositol phosphates did not increase but instead decreased with GRF. There was a small but significant reduction of labeling of inositol trisphosphate (IP3) at 90 min of GRF incubation. There were also small but significant decreases in 32P incorporation into inositol bisphosphate (IP2) at 0.33, 3, and 30 min. GRF did not significantly alter 32P labeling of inositol monophosphate (IP). These results indicate that GRF does not stimulate phospholipase C activity in somatotrophs. We conclude that the phosphatidylinositol second messenger system does not play an essential role in the action of GRF.

摘要

我们研究了磷脂酰肌醇系统在生长激素释放因子(GRF)作用中的角色。我们通过测定GRF诱导纯化大鼠生长激素分泌细胞中单个磷酸肌醇和肌醇磷酸的32P标记变化,来探究GRF是否刺激磷脂酶C的活性。用GRF(10^(-7)M)刺激生长激素分泌细胞0.33、1、3、10、30和90分钟。GRF并未显著且持续地改变32P掺入磷脂酰肌醇二磷酸(PIP2)、磷脂酰肌醇单磷酸(PIP)或磷脂酰肌醇(PI)的情况,不过在90分钟时PIP标记有小幅减少。总体而言,GRF作用下,32P掺入肌醇磷酸的水平并未增加,反而降低。在GRF孵育90分钟时,肌醇三磷酸(IP3)的标记有小幅但显著的减少。在0.33、3和30分钟时,32P掺入肌醇二磷酸(IP2)也有小幅但显著的减少。GRF并未显著改变肌醇单磷酸(IP)的32P标记。这些结果表明GRF不会刺激生长激素分泌细胞中的磷脂酶C活性。我们得出结论,磷脂酰肌醇第二信使系统在GRF的作用中不发挥重要作用。

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