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作 者:李晓东[1] 李英[1] 丁新国[2] 张红梅[2] 高山林[2] 郭志军[2]
机构地区:[1]河北医科大学第三医院肾内科,石家庄050051 [2]唐山市工人医院肾内科
出 处:《中华肾脏病杂志》2010年第6期448-452,共5页Chinese Journal of Nephrology
摘 要:目的 研究甲状旁腺素(PTH)对人肾小管上皮细胞(HK-2)合成分泌Ⅲ型胶原、纤连蛋白以及对纤溶酶原激活物抑制物1(PAI-1)、基质金属蛋白酶1(MMP-1)、金属蛋白酶1组织抑制剂(TIMP-1)基因表达的影响,以探讨PTH在肾间质纤维化发病机制中的作用.方法 HK-2细胞培养于含5%FBS的DMEM-F12培养液中,加入终浓度为0、10^-12、10^-11、10^-10、10^-9、10^-8 mol/L PTH的培养液刺激HK-2细胞48 h,或10^-8 mol/L PTH刺激HK-2细胞不同时间(0、12、24、48、72 h).应用半定量RT-PCR法检测细胞中Ⅲ型胶原、纤连蛋白、PAI-1、MMP-1、TIMP-1基因的表达;Western印迹法检测HK-2细胞中Ⅲ型胶原的蛋白表达;ELISA法检测细胞培养上清液中纤连蛋白的含量.结果 PTH呈剂量和时间依赖性促进HK-2细胞中Ⅲ型胶原、纤连蛋白、PAI-1、TIMP-1 mRNA的表达,抑制MMP-1 mRNA的表达,MMP-1/TIMP-1比值降低.PTH呈剂量和时间依赖性增加HK-2细胞中Ⅲ型胶原的蛋白表达及细胞培养上清液中纤连蛋白的含量.结论 PTH通过促进HK-2细胞中PAI-1、TIMP-1的基因表达,抑制MMP-1的基因表达,导致细胞外基质合成增加而降解减少.Objective To investigate the effects of parathyroid hormone (PTH) on the synthesis and secretion of collagen Ⅲ and fibronectin (FN), and the expressions of plasminogen activator inhibitor-1 (PAI-1), matrix metalloproteinase-1 (MMP-1) and tissue inhibitor of metalloproteinase-1 (TIMP-1) mRNA in cultured human renal tubular epithelial cells (HK-2).Methods HK-2 cells were cultured in DMEM-F12 medium supplemented with 5% FBS. Cells were exposed to different concentrations of PTH (0, 10^-12, 10^-11, 10^-10, 10^-9, 10^-8 mol/L) for 48 h, or 10^-8 mol/L PTH at different time (0, 12, 24, 48, 72 h). The gene expressions of collagen Ⅲ,FN, PAI-1, MMP-1, and TIMP-1 were detected by semi-quantitative RT-PCR. The protein expression of collagen Ⅲ was detected by Western blotting. The level of FN in the supernatant was assayed by enzyme linked immunosorbent assay (ELISA). Results PTH increased gene expressions of collagen Ⅲ, FN, PAI-1 and TIMP-1 in a dose- and time-dependent manner, but decreased MMP-1 gene expression. Then the ratio of MMP-1/TIMP-1 was decreased. PTH increased the collagen Ⅲ protein expression in cultured HK-2 cells and the level of FN in the supernatant of cultured HK-2 cells in a dose- and time-dependent manner. Conclusion PTH can up-regulate PAI-1, TIMP-1 gene expressions, and down-regulate MMP-1 gene expression,resulting in elevation of extracellular matrix (ECM) synthesis and reductim of degradation.
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