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机构地区:[1]东南大学附属中大医院内分泌科,南京210009 [2]江苏省人民医院内分泌科
出 处:《中国糖尿病杂志》2009年第3期219-221,共3页Chinese Journal of Diabetes
基 金:江苏省教育厅高校自然科学研究项目(02KJA320001);教育部教学研究重点项目(204051)
摘 要:目的观察糖基化终产物(AGEs)对人肾小球系膜细胞(HRMC)膜上β1整合素及其胞内靶点黏着斑激酶(FAK)表达的影响。方法用不同浓度的AGE-BSA干预培养的HRMC;RT-PCR法测定细胞β1整合素和FAK的mRNA水平;western Blot法检测β1整合素和FAK的蛋白表达。结果在50至400mg/L浓度范围内,AGE-BSA组β1整合素、FAK mRNA及蛋白表达均较对照组增加(P<0.05)。结论一定范围内,AGEs呈浓度依赖性上调β1整合素及其下游信号分子FAK mRNA及蛋白表达,这可能是AGEs致糖尿病肾病的一个重要机制。Objective To investigate the effects of advanced glycation end products (AGEs) on the expressions of β1-integrin and FAK in cultured human renal mesangiai cells (HRMC). Methods HRMC were incubated with AGEs-modified bovine serum albumin (AGE-BSA), the mRNA expressions of β1- integrin and FAK in HRMC were analyzed by use of RT-PCR,and the protein expressions of β1-integrin and FAK in HRMC were determined by Western blot. Results The levels of β1-integrin and FAK mRNA and protein in HRMC incubated with AGE-BSA were significantly higher than those in normal control (P〈0. 05). Conclusions AGEs up-regulate the expression of β1-integrin and FAK in HRMC, which might have potential implications of the pathogenic mechanism of diabetic nephropathy.
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