Dionne S, D'Agata I D, Ruemmele F M, Levy E, St-Louis J, Srivastava A K, Levesque D, Seidman E G
Department of Pediatrics, Ste-Justine Hospital, Montreal, Quebec, Canada.
Biochem Biophys Res Commun. 1998 Jan 6;242(1):146-50. doi: 10.1006/bbrc.1997.7922.
The role of TNF-alpha in modulating intestinal crypt cell growth was examined, in comparison with EGF. Both significantly increased IEC-6 cell proliferation. Neither EGF nor TNF-alpha overcame the inhibitory effect on growth exerted by the tyrosine kinase inhibitor genistein. Immunoblots with phosphotyrosine antibodies showed increased tyrosine phosphorylation of IEC-6 cell proteins in response to EGF and TNF-alpha stimulation. TNF-alpha increased ERK1 and ERK2 MAPK phosphorylation. A MAPK assay confirmed the increased activity upon TNF-alpha stimulation. Selective inhibition of MAPK activation by PD98059 resulted in a dose dependent inhibition of TNF-alpha or EGF-induced IEC-6 cell growth. These findings suggest a role for TNF-alpha in the regulation of intestinal epithelial cell growth and that the mitogenic effect of TNF-alpha requires protein tyrosine phosphorylation and MAPK activation.
与表皮生长因子(EGF)相比,研究了肿瘤坏死因子-α(TNF-α)在调节肠隐窝细胞生长中的作用。二者均显著增加了IEC-6细胞的增殖。EGF和TNF-α均未克服酪氨酸激酶抑制剂染料木黄酮对生长的抑制作用。用磷酸酪氨酸抗体进行的免疫印迹显示,响应于EGF和TNF-α刺激,IEC-6细胞蛋白的酪氨酸磷酸化增加。TNF-α增加了细胞外调节蛋白激酶1(ERK1)和细胞外调节蛋白激酶2(ERK2)的丝裂原活化蛋白激酶(MAPK)磷酸化。一项MAPK分析证实了TNF-α刺激后活性增加。PD98059对MAPK激活的选择性抑制导致对TNF-α或EGF诱导的IEC-6细胞生长的剂量依赖性抑制。这些发现表明TNF-α在肠上皮细胞生长调节中起作用,并且TNF-α的促有丝分裂作用需要蛋白质酪氨酸磷酸化和MAPK激活。