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The involvement of p38 MAPK in transforming growth factor β1-induced apoptosis in murine hepatocytes

查看全文 作  者:[1]LiaoJH;[2]ChenJS 高影响力作者 机构地区:[1]StateKeyLaboratoryofMolecularBiology,InstituteofBiochemistryandCellBiology,ShanghaiInstitutesforBiologicalSciences,ChineseAcademyofSciences,320YueYangRoad,Shanghai200031,China;[2]StateKeyLaboratoryofMole高影响力机构 出  处:《Cell Research》索引2001年第11卷第2期,共6页高影响力期刊 基  金:grants fromthe Chinese Academy of Sciences (No. KJ951-BI608), the National Natural Sciences FOundation ofChina (No. 39625007 and 摘  要:We reported in this manuscript that TGF-β1 induces apoptosis in AML12 murine hepatocytes, which is associated with the activation of p38 MAPK signaling pathway. SB202190, a specific inhibitor of p38 MAPK, strongly inhibited the TGF-β1-induced apoptosis and PAI-1 promoter activity. Treatment of cells with TGF-β1 activates p38. Furthermore, over-expression of dominant negative mutant p38 also reduced the TGF-β1-induced apoptosis. The data indicate that the activation of p38 is involved in TGF-β1-mediated gene expression and apoptosis. 关 键 词:转化生长因子Β 细胞凋亡 P38 肝细胞 信号传导
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