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作 者:李萍[1] 梁琳琅[1] 杨威[1] 杨昕[1] 张颖[1] 向军[2]
机构地区:[1]沈阳军区总医院内分泌科,辽宁沈阳110016 [2]沈阳军区总医院泌尿外科,辽宁沈阳110016
出 处:《中国组织化学与细胞化学杂志》2009年第6期687-691,共5页Chinese Journal of Histochemistry and Cytochemistry
摘 要:目的探讨血凝素样氧化低密度脂蛋白受体1(LOX-1)在D-葡萄糖诱导人肾小球系膜细胞表达转化生长因子β1(TGF-β1)中的作用。方法在体外培养人肾小球系膜细胞,在不同时间加入不同浓度的D-葡萄及LOX-1特异性阻滞剂JTX92,用半定量RT-PCR法检测LOX-1和TGF-β1基因表达的相对含量,用Western blot法检测p38 MAPK蛋白质的相对含量,用酶联免疫吸附法(ELISA)检测细胞培养液中TGF-β1浓度。结果D-葡萄糖以时间和浓度依赖的方式增加细胞内LOX-1和TGF-β1 mRNA表达和培养液中TGF-β1浓度,同时也以时间和浓度依赖的方式增加p38 MAPK的表达,JTX92可以明显抑制LOX-1、TGF-β1和p38 MAPK的表达。结论高浓度D-葡萄糖可能通过上调LOX-1的表达,激活细胞内的p38 MAPK信号传递途径,促使人肾小球系膜细胞合成并分泌大量TGF-β1,参与糖尿病肾病的发生发展。Objective To study the role of lectin-like oxidized low-density lipoprotein receptor-1(LOX-1) in the expression of transforming growth factor-β1(TGF-β1) induced by D-Glucose in human glomerular mesangial cells.MethodsHuman glomerular mesangial cells were incubated with D-Glucose(100 to 600mg/dl) for 6 to 48 hour and pretreated with JTX92(10ug/ml),a blocking antibody to LOX-1,before exposure to D-Glucose.The expression of LOX-1 and TGF-β1 mRNA was determined by reverse transcriptase polymerase chain reaction.Western blot was used to detect the activity of p38MAPK.The level of TGF-β1 protein was measured by enzyme-linked immunosorbent assay.ResultsD-Glucose increased the expression of TGF-β1mRNA and protein、LOX-1 mRNA and p38MAPK activity in a concentration-and time-dependent manner,which was inhibited by JTX92.The effect of D-Glucose was mediated by the scavenger receptor LOX-1,because pretreatment of HGMC with JTX92 prevented the expression of TGF-β1、LOX-1 and p38MAPK in response to D-Glucose(P〈 0.01).ConclusionD-glucose can increase the expression of TGF-β1 mRNA and the synthesis and secretion of TGF-β1 protein by upregulating LOX-1 and activating p38MAPK signal pathway in human glomerular mesangial cells.
关 键 词:D-葡萄糖 血凝素样氧化低密度脂蛋白受体1 p38MAPK信号传递途径 人肾小球系膜细胞
分 类 号:R322.61[医药卫生—人体解剖和组织胚胎学]
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