Hirokawa M, Miura S, Kishikawa H, Yoshida H, Nakamizo H, Higuchi H, Nakatsumi R C, Suzuki H, Saito H, Ishii H
Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
Dig Dis Sci. 2001 Sep;46(9):1993-2003. doi: 10.1023/a:1010607819842.
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.
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。