G-PROTEIN REGULATION OF CAPACITATIVE CALCIUM-ENTRY MAY BE MEDIATED BY PROTEIN-KINASE-A AND PROTEIN-KINASE-C IN XENOPUS OOCYTES

被引:52
作者
PETERSEN, CCH
BERRIDGE, MJ
机构
[1] Babraham Inst Lab Molec Signalling, Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, Downing Street
基金
英国惠康基金;
关键词
D O I
10.1042/bj3070663
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Inositol 2,4,5-trisphosphate irreversibly activated capacitative calcium entry in Xenopus oocytes, whereas guanosine thiotriphosphate (GTP[S]) and AlF4- only activated capacitative calcium entry transiently. Both GTP[S] and AIF(4)(-) inhibited capacitative calcium entry activated by thapsigargin pretreatment, but guanosine thiodiphosphate (GDP[S]), inositol 2,4,5-trisphosphate and dibutyryl cyclic GMP did not affect capacitative calcium entry. This suggests the involvement of heterotrimeric GTP-binding proteins in the regulation of capacitative calcium entry. Activation of protein kinase C or cyclic-AMP-dependent protein kinase had profound effects on capacitative calcium entry, which were consistent with the hypothesis that the effects of GTP[S] and AlF4- on capacitative calcium entry may be mediated via heterotrimeric GTP-binding protein stimulation of kinases. Further evidence for this hypothesis was derived from the result that the effects of GTP[S] on calcium entry could be inhibited by the application of the protein kinase inhibitor staurosporine.
引用
收藏
页码:663 / 668
页数:6
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