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机械压力加载可激活肠上皮细胞中的丝裂原活化蛋白激酶和早期即刻基因。

Loading of mechanical pressure activates mitogen-activated protein kinase and early immediate gene in intestinal epithelial cells.

作者信息

Hirokawa M, Miura S, Kishikawa H, Yoshida H, Nakamizo H, Higuchi H, Nakatsumi R C, Suzuki H, Saito H, Ishii H

机构信息

Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.

出版信息

Dig Dis Sci. 2001 Sep;46(9):1993-2003. doi: 10.1023/a:1010607819842.

Abstract

Intestinal mucosa is continuously exposed to mechanical forces. We examined whether pressure loading activates mitogen-activated protein kinase (MAPK) and expression of early immediate genes in intestinal epithelial cells. Pressure was applied to IEC18 cells by helium gas in a culture flask and pressure-induced cell proliferation was examined. The expression of early immediate genes, MAPK activity, and activation of nuclear factor activator protein-1 (AP-1) were also examined. Pressures significantly promoted cell proliferation with peak effect at 80 mm Hg. Pretreatment with either a protein kinase C inhibitor or tyrosine kinase inhibitors, but not calcium chelating agents significantly inhibited cell proliferation promoted by pressure. Early inductions of c-myc and c-fos proteins, increased activity of MAPK, and activation of AP-1 were observed by pressure loading. Our study showed that intestinal mucosal cell proliferation is promoted by mechanical pressure and various intracellular signaling pathways are involved in the process.

摘要

肠黏膜持续受到机械力作用。我们研究了压力负荷是否会激活丝裂原活化蛋白激酶(MAPK)以及肠道上皮细胞中早期即刻基因的表达。通过在培养瓶中用氦气对IEC18细胞施加压力,并检测压力诱导的细胞增殖情况。同时还检测了早期即刻基因的表达、MAPK活性以及核因子活化蛋白-1(AP-1)的激活情况。压力显著促进细胞增殖,在80毫米汞柱时达到峰值效应。用蛋白激酶C抑制剂或酪氨酸激酶抑制剂预处理,但钙螯合剂预处理则不能显著抑制压力促进的细胞增殖。压力负荷可观察到c-myc和c-fos蛋白的早期诱导、MAPK活性增加以及AP-1的激活。我们的研究表明,机械压力可促进肠黏膜细胞增殖,且该过程涉及多种细胞内信号通路。

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