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Expression of tissue inhibitor of matrix metalloproteinases-1 during aging in rat liver

机译:大鼠肝脏衰老过程中基质金属蛋白酶-1组织抑制剂的表达

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AIM: To investigate the expression and role of tissue inhibitor of matrix metalloproteinases-1 (TIMP-1) during natural aging in rat liver and to detect the expression of matrix metalloproteinase-2 (MMP-2) and MMP-9. METHODS: The rats were divided into 3-mo-old group (n = 5), 10-mo-old group (n = 5) and 24-mo-old group (n = 5). Histopathologic changes of liver were observed with HE and Masson stain. The location and protein expressions of TIMP-1 were determined by immunohistochemistry and Western blot; message RNA (mRNA) levels were measured in livers from rats of various ages by semi-quantitative reverse transcriptional polymerase chain reaction (RT-PCR). In addition, the expression of MMP-2 and MMP-9 was assessed by RT-PCR and Western blot. RESULTS: Histologic examination showed that the aging liver had excessive fatly degeneration and collagen deposition. Immunohistochemical staining showed that TIMP-1 related antigen in livers was located in cytoplasm. The protein expression of TIMP-1 was significantly higher in the oldest animals and the mRNA expression was increased significantly in the 24-mo-old rats (t = 4.61, P= 0.002<0.05, 24- vs 10-mo-old rats; t = 4.31, P= 0.003<0.05, 24- vs 3-mo-old rats). The expression of MMP-2 and MMP-9 had no change during aging; the ratios 1/MMP-2 and TIMP-1/MMP-9 in aging liver were significantly higher than those in maturation and young livers. CONCLUSION: TIMP-1 may play an important role in the process of liver aging.
机译:目的:研究组织金属蛋白酶-1(TIMP-1)组织抑制剂在大鼠肝脏自然衰老过程中的表达及其作用,并检测基质金属蛋白酶-2(MMP-2)和MMP-9的表达。方法:将大鼠分为3个月龄组(n = 5),10个月龄组(n = 5)和24个月龄组(n = 5)。用HE和Masson染色观察肝脏的组织病理学变化。免疫组织化学和Western blot检测TIMP-1的位置和蛋白表达。通过半定量逆转录聚合酶链反应(RT-PCR)测量来自不同年龄大鼠的肝脏中的message RNA(mRNA)水平。另外,通过RT-PCR和Western印迹评估MMP-2和MMP-9的表达。结果:组织学检查显示衰老的肝脏具有过多的脂肪变性和胶原沉积。免疫组织化学染色显示肝脏中TIMP-1相关抗原位于细胞质中。在24岁大的大鼠中,TIMP-1的蛋白表达显着较高,而在24岁大的大鼠中,mRNA表达则显着增加(t = 4.61,P = 0.002 <0.05,24岁和10岁的大鼠; t = 4.31,P = 0.003 <0.05,对于24个月和3个月大的大鼠)。 MMP-2和MMP-9的表达在衰老过程中没有变化。衰老肝脏中1 / MMP-2和TIMP-1 / MMP-9的比率显着高于成熟肝脏和年轻肝脏。结论:TIMP-1可能在肝衰老过程中起重要作用。

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