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Expression of TIMP-1 and TIMP-2 in rats with hepatic fibrosis

机译:TIMP-1和TIMP-2在肝纤维化大鼠中的表达

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AIM: To investigate the location and expression of TIMP-1 and TIMP-2 in the liver of normal and experimental hepatic fibrosis in rats. METHODS: The rat models of experimental immunity hepatic fibrosis (n=20) were prepared by the means of immunologic attacking with human serum albumin (HSA), and normal rats (n=10) served as control group. Both immunohistochemistry and in situ hybridization methods were respectively used to detect the TIMP-1 and TIMP-2 mRNA and related antigens in liver. The liver tissue was detected to find out the gene expression of TIMP-1 and TIMP-2 with RT-PCR. RESULTS: The TIMP-1 and TIMP-2 related antigens in livers of experimental group were expressed in myofibroblasts and fibroblasts (TIMP-1: 482+-65 vs 60+-20; TIMP-2: 336+-48 vs 50+-19, P<0.001). This was the most obvious in portal area and fibrous septum. The positive signals were located in cytoplasm, not in nucleus. Such distribution and location were confirmed by situ hybridization (TIMP-1/β-actin: 1.86+-0.47 vs 0.36+-0.08; TIMP-2/β-actin: 1.06+-0.22 vs 0.36+-0.08, P<0.001). The expression of TIMP-1 and TIMP-2 was seen in the liver of normal rats, but the expression level was very low. However, the expression of TIMP-1 and TIMP-2 in the liver of experimental group was obviously high. CONCLUSION: In the process of hepatic fibrosis, fibroblasts and myofibroblasts are the major cells that express TIMPs. The more serious the hepatic fibrosis is in the injured liver, the higher the level of TIMP-1 and TIMP-2 gene expression.
机译:目的:探讨正常和实验性肝纤维化大鼠肝脏中TIMP-1和TIMP-2的定位和表达。方法:采用人血清白蛋白(HSA)免疫攻击法制备实验性免疫性肝纤维化大鼠模型(n = 20),以正常大鼠(n = 10)为对照组。分别采用免疫组化和原位杂交方法检测肝脏中TIMP-1和TIMP-2 mRNA及相关抗原。 RT-PCR检测肝组织,以发现TIMP-1和TIMP-2的基因表达。结果:实验组肝脏TIMP-1和TIMP-2相关抗原在成肌纤维细胞和成纤维细胞中表达(TIMP-1:482 + -65 vs 60 + -20; TIMP-2:336 + -48 vs 50 +- 19,P <0.001)。这在门静脉区域和纤维间隔中最为明显。阳性信号位于细胞质中,而不位于细胞核中。通过原位杂交证实了这种分布和位置(TIMP-1 /β-肌动蛋白:1.86 + -0.47对0.36 + -0.08; TIMP-2 /β-肌动蛋白:1.06 + -0.22对0.36 + -0.08,P <0.001) 。在正常大鼠肝脏中可见TIMP-1和TIMP-2的表达,但表达水平很低。然而,实验组肝脏中TIMP-1和TIMP-2的表达明显较高。结论:在肝纤维化过程中,成纤维细胞和成肌纤维细胞是表达TIMPs的主要细胞。受损肝中的肝纤维化越严重,TIMP-1和TIMP-2基因表达的水平越高。

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