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大鼠肾小球系膜细胞中反复的拉伸和松弛循环对S6激酶的激活。蛋白激酶C参与的证据。

Activation of S6 kinase by repeated cycles of stretching and relaxation in rat glomerular mesangial cells. Evidence for involvement of protein kinase C.

作者信息

Homma T, Akai Y, Burns K D, Harris R C

机构信息

Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee 37232.

出版信息

J Biol Chem. 1992 Nov 15;267(32):23129-35.

PMID:1429660
Abstract

Quiescent rat glomerular mesangial cells were exposed to repeated cycles of stretching and relaxation, and the effects on the rate of collagen production, proliferation, and S6 kinase activity were investigated. Stretch/relaxation induced increases in production of both collagen and non-collagenous proteins. Proliferation of mesangial cells was stimulated by stretch/relaxation and epidermal growth factor, but not by angiotensin II; however, administration of angiotensin II augmented stretch/relaxation-induced cell proliferation. Cytosolic S6 kinase activity was stimulated by stretch/relaxation, angiotensin II, epidermal growth factor, or phorbol 12-myristate 13-acetate. The increased S6 kinase activity was detectable within 30 min after initiation of stretch/relaxation and was blocked by either inhibitors of protein kinase C or prior down-regulation of protein kinase C following prolonged incubation with phorbol 12-myristate 13-acetate. Both translocation of protein kinase C from the cytosolic to the membrane fraction and phosphorylation of an endogenous 80-kDa protein were observed within 5 min of initiation of stretch/relaxation. These results demonstrate that in mesangial cells, mechanical factors alone can induce increases in production of collagen and non-collagenous proteins and in cell proliferation. The observation that stretch/relaxation induced stimulation of S6 kinase activity through protein kinase C-dependent mechanisms suggests that activation of protein kinase C may be a key event in initiating adaptive responses of mesangial cells to increased workload.

摘要

将静止的大鼠肾小球系膜细胞暴露于反复的拉伸和松弛循环中,研究其对胶原蛋白生成速率、细胞增殖和S6激酶活性的影响。拉伸/松弛诱导胶原蛋白和非胶原蛋白生成增加。系膜细胞的增殖受到拉伸/松弛和表皮生长因子的刺激,但不受血管紧张素II的刺激;然而,给予血管紧张素II可增强拉伸/松弛诱导的细胞增殖。胞质S6激酶活性受到拉伸/松弛、血管紧张素II、表皮生长因子或佛波醇12-肉豆蔻酸酯13-乙酸酯的刺激。拉伸/松弛开始后30分钟内即可检测到S6激酶活性增加,并且可被蛋白激酶C抑制剂或在用佛波醇12-肉豆蔻酸酯13-乙酸酯长时间孵育后预先下调蛋白激酶C所阻断。在拉伸/松弛开始后5分钟内观察到蛋白激酶C从胞质向膜部分的转位以及一种内源性80 kDa蛋白的磷酸化。这些结果表明,在系膜细胞中,仅机械因素就能诱导胶原蛋白和非胶原蛋白生成增加以及细胞增殖。拉伸/松弛通过蛋白激酶C依赖性机制诱导S6激酶活性刺激这一观察结果表明,蛋白激酶C的激活可能是启动系膜细胞对增加的工作负荷的适应性反应的关键事件。

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