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作 者:李萍[1] 张海燕[1] 盛志业[2] 刘国良[1]
机构地区:[1]中国医科大学附属第一医院内分泌科,辽宁沈阳110001 [2]沈阳军区总医院内分泌科
出 处:《中国医科大学学报》2007年第1期23-26,共4页Journal of China Medical University
基 金:辽宁省重点科技攻关基金资助项目(2001225004)
摘 要:目的:探讨血凝素样氧化低密度脂蛋白受体1(LOX-1)在氧化低密度脂蛋白(ox-LDL)诱导人肾小球系膜细胞(HGMC)表达转化生长因子(TGF-β1)中的作用。方法:体外培养HGMC,在不同时间加入不同浓度的ox-LDL及LOX-1阻滞性抗体JTX92,用半定量RT-PCR法检测细胞LOX-1和TGF-β1mRNA表达,用Westernblot法检测细胞LOX-1蛋白合成,用酶联免疫吸附法(ELISA)检测细胞培养液中TGF-β1浓度。结果:ox-LDL以时间和浓度依赖的方式增加LOX-1mRNA和蛋白表达的同时,也以时间和浓度依赖的方式增加细胞内TGF-β1mRNA表达和培养液中TGFβ1蛋白的含量,JTX92(10μg/ml)可以明显抑制LOX-1和TGF-β1的表达(P<0.01)。结论:ox-LDL通过激活LOX-1调节HGMCTGF-β1基因表达、蛋白合成与分泌。Objective:To study the role of lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1), the specific scavenger receptor for oxidized low-density hpoprotein (ox-LDL),in the expression of transforming growth factor-β1 (TGF-β1) induced by ox-LDL in human glomerular mesangial cells. Methods:Human glomerular mesangial cells were incubated with ox-LDL (10 to 80 μg/ml) for 6 to 24 hours and then pretreated with JTX92 (10 μg/ml),a blocking antibody to LOX-1 ,before exposed to ox-LDL. The expressions of LOX-1 and TGF- β1 mRNA and the expression of LOX-1 protein were detennined by reverse transcriptase polymerase chain reaction and Western blot, respectively. The level of TGF-β1 protein was measured by enzyme-linked immunosorbent assay.Results: ox-LDL increased the expressions of both LOX-1 and TGF-β1 mRNA and protein in a concentration-and time-dependent manner,which was inhibited by JTX92. The effect of ox-LDL was mediated by its scavenger receptor LOX-1 ,because the pretreatment of HGMC with a blocking antibody to LOX-1 prevented the expression of TGF β1 in response to ox-LDL (P 〈 0.01 ).Conclusion:ox-LDL may regulate the expression of TGF-β1 mRNA and the synthesis and secretion of TGF-β1 protein via activating LOX-1 in human glomerular mesangial cells.
关 键 词:血凝素样氧化低密度脂蛋白受体1 转化生长因子Β1 人肾小球系膜细胞 糖尿病肾病
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