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Ha-ras和v-mos对血清生长因子的Ca2+动员系统的脱敏作用。

Desensitization of the Ca2+-mobilizing system to serum growth factors by Ha-ras and v-mos.

作者信息

Maly K, Doppler W, Oberhuber H, Meusburger H, Hofmann J, Jaggi R, Grunicke H H

机构信息

Institute of Medical Chemistry and Biochemistry, University of Innsbruck, Austria.

出版信息

Mol Cell Biol. 1988 Oct;8(10):4212-6. doi: 10.1128/mcb.8.10.4212-4216.1988.

Abstract

An elevation of the intracellular pH and a rise in the cytoplasmic Ca2+ concentration are considered important mitogenic signals which are observed after stimulation by various growth factors. In a preceding report it was demonstrated that the expression of Ha-ras or v-mos in cells transfected with Ha-ras or v-mos, respectively, leads to an activation of the Na+/H+ antiporter and a concomitant rise in intracellular pH (W. Doppler, R. Jaggi, and B. Groner, Gene 54:145-151, 1987). This report describes the effect of the Ha-ras and v-mos oncogenes on intracellular Ca2+ release. The expression of Ha-ras in NIH 3T3 cells carrying a glucocorticoid-inducible transforming Ha-ras gene caused a desensitization of the Ca2+-mobilizing system to serum growth factors. The induction of p21ras in cells carrying the corresponding glucocorticoid-inducible proto-oncogene did not affect the Ca2+ response to growth factors. Conditions leading to the expression of the transforming Ha-ras gene but not those causing the induction of the normal Ha-ras gene yielded an increase in phosphatidylinositol turnover and a concomitant rise in inositol phosphates. Results similar to those obtained with the transforming Ha-ras gene were seen after the expression of v-mos. The data are consistent with a mechanism in which expression of the transforming Ha-ras gene leads to a release of Ca2+ from intracellular stores via elevated levels of inositol trisphosphate.

摘要

细胞内pH值升高和细胞质Ca2+浓度升高被认为是重要的促有丝分裂信号,在各种生长因子刺激后均可观察到。在之前的一份报告中表明,分别用Ha-ras或v-mos转染的细胞中Ha-ras或v-mos的表达会导致Na+/H+反向转运体的激活以及细胞内pH值的随之升高(W.多普勒、R.贾吉和B.格罗纳,《基因》54:145 - 151,1987)。本报告描述了Ha-ras和v-mos癌基因对细胞内Ca2+释放的影响。在携带糖皮质激素诱导型转化Ha-ras基因的NIH 3T3细胞中Ha-ras的表达导致Ca2+动员系统对血清生长因子脱敏。在携带相应糖皮质激素诱导型原癌基因的细胞中诱导p21ras不会影响对生长因子的Ca2+反应。导致转化Ha-ras基因表达的条件而非那些导致正常Ha-ras基因诱导的条件会使磷脂酰肌醇周转率增加以及肌醇磷酸随之升高。在v-mos表达后观察到与用转化Ha-ras基因获得的结果相似的结果。这些数据与一种机制一致,即转化Ha-ras基因的表达通过升高的肌醇三磷酸水平导致细胞内储存的Ca2+释放。

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