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Effect of transforming growth factor beta and bone morphogenetic proteins on rat hepatic stellate cell proliferation and transdifferentiation 被引量:17

Effect of transforming growth factor beta and bone morphogenetic proteins on rat hepatic stellate cell proliferation and transdifferentiation
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摘要 AIM: To explore different roles of TGF-β (transforming growth factor beta) and bone morphogenetic proteins (BMPs)in hepatic stellate cell proliferation and trans-differentiation.METHODS: Hepatic stellate cells were isolated from male Sprague-Dawley rats. Sub-cultured hepatic stellate cells were employed for cell proliferation assay with WST-1 reagent and Western blot analysis with antibody against smooth muscle alpha actin (SMA).RESULTS: The results indicated that TGF-β1 significantly inhibited cell proliferation at concentration as low as 0.1 ng/ml, but both BMP-2 and BMP-4 did not affect cell proliferation at concentration as high as 10 ng/ml. The effect on hepatic stellate cell trans-differentiation was similar between TGFβ1 and BMPs. However, BMPs was more potent at transdifferentiation of hepatic stellate cells than TGF-β1. In addition, we observed that TGF-β1 transient reduced the abundance of SMA in hepatic stellate cells.CONCLUSION: TGF-β may be more important in regulation of hepatic stellate cell proliferation while BMPs may be the major cytokines regulating hepatic stellate cell transdifferentiation. AIM:To explore different roles of TGF-β(transforming growth factor beta)and bone morphogenetic proteins(BMPs) in hepatic stellate cell proliferation and trans-differentiation. METHODS:Hepatic stellate cells were isolated from male Sprague-Dawley rats.Sub-cultured hepatic stellate cells were employed for cell proliferation assay with WST-1 reagent and Western blot analysis with antibody against smooth muscle alpha actin(SMA). RESULTS:The results indicated that TGF-β1 significantly inhibited cell proliferation at concentration as low as 0.1 ng/ ml,but both BMP-2 and BMP-4 did not affect cell proliferation at concentration as high as 10 ng/ml.The effect on hepatic stellate cell trans-differentiation was similar between TGF- β1 and BMPs.However,BMPs was more potent at trans- differentiation of hepatic stellate cells than TGF-β1.In addition,we observed that TGF-β1 transient reduced the abundance of SMA in hepatic stellate cells. CONCLUSION:TGF-β may be more important in regulation of hepatic stellate cell proliferation while BMPs may be the major cytokines regulating hepatic stellate cell trans- differentiation.
出处 《World Journal of Gastroenterology》 SCIE CAS CSCD 2003年第4期784-787,共4页 世界胃肠病学杂志(英文版)
关键词 ANIMALS Bone Morphogenetic Proteins Cell Differentiation Cell Division Cells Cultured Liver Male RATS Rats Sprague-Dawley Research Support Non-U.S. Gov't Transforming Growth Factor beta 转化生长因子β 骨形态发生蛋白 肝星形细胞 细胞增殖 细胞分化 细胞转换 丝氨酸-苏氨酸激激酶
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