Akai Y, Homma T, Burns K D, Yasuda T, Badr K F, Harris R C
Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee.
Am J Physiol. 1994 Aug;267(2 Pt 1):C482-90. doi: 10.1152/ajpcell.1994.267.2.C482.
In cultured rat glomerular mesangial cells, continuous cycles of stretching and relaxation (stretch/relaxation) stimulate cell proliferation, protein synthesis, and prostaglandin production. We examined regulation of gene expression that may underlie these alterations in cell functions. Stretch/relaxation caused time-dependent induction of the immediate early genes, c-fos and zif 268/egr-1, with maximal increases occurring between 15 and 30 min. The mitogen-inducible prostaglandin G2/H2 synthase (PGH2S-2) gene was also induced within 30 min of stretch/relaxation, with concomitant increases in the immunoreactive PGH2S-2 protein. These gene inductions were preceded by transient translocation of protein kinase C activity from cytosol to membrane as well as by increases in 45Ca2+ uptake and total cellular calcium content. The stretch/relaxation-induced expression was suppressed by protein kinase C inhibition, whereas less profound inhibition was observed with inhibition of calcium influx in low (100 nM) calcium buffer. These findings indicate that in mesangial cells mechanical stress induces expression of the protooncogenes and the mitogen-inducible cyclooxygenase primarily through protein kinase C-dependent mechanisms.
在培养的大鼠肾小球系膜细胞中,持续的拉伸和松弛循环(拉伸/松弛)刺激细胞增殖、蛋白质合成和前列腺素生成。我们研究了可能是这些细胞功能改变基础的基因表达调控。拉伸/松弛导致即时早期基因c-fos和zif 268/egr-1的时间依赖性诱导,在15至30分钟之间出现最大增加。有丝分裂原诱导的前列腺素G2/H2合酶(PGH2S-2)基因在拉伸/松弛30分钟内也被诱导,同时免疫反应性PGH2S-2蛋白增加。这些基因诱导之前,蛋白激酶C活性从细胞质短暂转位到细胞膜,以及45Ca2+摄取和细胞总钙含量增加。蛋白激酶C抑制可抑制拉伸/松弛诱导的表达,而在低钙(100 nM)缓冲液中抑制钙内流时观察到的抑制作用较弱。这些发现表明,在系膜细胞中,机械应力主要通过蛋白激酶C依赖性机制诱导原癌基因和有丝分裂原诱导的环氧化酶的表达。