首页> 外文期刊>Journal of Huazhong University of Science and Technology >Expression of Connective Tissue Growth Factor in Renal Tubulointerstitial Fibrosis in Rats and Its Pathogenic Role
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Expression of Connective Tissue Growth Factor in Renal Tubulointerstitial Fibrosis in Rats and Its Pathogenic Role

机译:结缔组织生长因子在大鼠肾小管间质纤维化中的表达及其致病作用

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In order to explore the role of connective tissue growth factor (CTGF) in the pathogene-sis of renal tubulointerstitial fibrosis, 48 Wistar rats were randomly divided into sham-operated and unilateral ureteral obstruction (UUO) group. On the postoperative day 1,3,7 and 14, the rats were killed and the kidneys were removed. The renal tubulointerstitial injury index was evaluated according to the MASSON staining. The mRNA levels of CTGF, transforming growth factor-β1 (TGF-β1), collagen Ⅰ (col ?), and plasminogen activator inhibitor-1 (PAI-1) were detected using reverse transcriptional-polymerase chain reaction (RT-PCR). Immunohistochemistry was performed to evaluate the protein expression of the above factors, and the relations among them were analyzed. Quantitative expression of CTGF protein in the kidneys was also assessed using Western blot. The results showed that TGF-β1 mRNA level was increased at first day after UUO, followed by a marked elevation of CTGF mRNA level, which began to increase 3 days after UUO (P < 0.01). With the progression of the disease, the mRNA expression of CTGF, col Ⅰ and PAI-1 was increased progressively. Immunohistochemistry revealed that the CTGF protein expression was significantly increased in fibrotic areas and tubular epithelial cells 3 days after UUO. On the post-UUO day 7, the protein level of CTGF was positively related to the renal tubulointerstitial injury index (r = 0.62, P < 0.01), the expression of TGF-β1 0 = 0.85, P < 0.01), col Ⅰ (r = 0.78, P < 0.01), and PAI-1(r = 0.76, P < 0.01). Upon Western blot analysis, CTGF protein expression began to increase 3 days after UUO, and appeared progressively throughout the time course (P < 0.01, as compared with sham-operated group). It is concluded that CTGF can be induced by TGF-β and mediate various profibrotic actions of this cytokine, such as increasing extracellular matrix (ECM) synthesis and decreasing ECM degradation. The increased expression of CTGF may play a crucial role in the development and progression of tubulointerstitial fibrosis.
机译:为了探讨结缔组织生长因子(CTGF)在肾小管间质纤维化病因中的作用,将48只Wistar大鼠随机分为假手术组和单侧输尿管阻塞(UUO)组。在术后第1、3、7和14天,处死大鼠并取出肾脏。根据MASSON染色评估肾小管间质损伤指数。使用逆转录聚合酶链反应(RT-PCR)检测CTGF,转化生长因子β1(TGF-β1),胶原Ⅰ(col col)和纤溶酶原激活物抑制剂1(PAI-1)的mRNA水平。 。进行免疫组织化学评价上述因子的蛋白表达,并分析它们之间的关系。还使用蛋白质印迹法评估了CTGF蛋白在肾脏中的定量表达。结果显示,UUO后第一天TGF-β1mRNA水平升高,随后CTGF mRNA水平显着升高,UUO后3天开始升高(P <0.01)。随着疾病的发展,CTGF,colⅠ和PAI-1的mRNA表达逐渐增加。免疫组织化学显示,UUO后3天,CTGF蛋白表达在纤维化区域和肾小管上皮细胞中显着增加。在UUO后第7天,CTGF的蛋白水平与肾小管间质损伤指数呈正相关(r = 0.62,P <0.01),TGF-β10 = 0.85,P <0.01),colⅠ( r = 0.78,P <0.01)和PAI-1(r = 0.76,P <0.01)。经Western blot分析,UUO后3天,CTGF蛋白表达开始增加,并在整个时间过程中逐渐出现(与假手术组相比,P <0.01)。结论是,TGF-β可以诱导CTGF并介导该细胞因子的各种纤维化作用,例如增加细胞外基质(ECM)的合成和减少ECM的降解。 CTGF的表达增加可能在肾小管间质纤维化的发生和发展中起关键作用。

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