Department of Pediatrics, The First Affiliated Hospital of Anhui Medical University, No. 218 Ji-Xi Road, Hefei, 230022, People's Republic of China.
Mol Biol Rep. 2013 Feb;40(2):1429-41. doi: 10.1007/s11033-012-2186-7. Epub 2012 Oct 17.
Although the mechanism underlying C-type natriuretic peptide (CNP) beneficial effects is not entirely understood, modulating the expression of matrix metalloproteinases (MMPs)/tissue inhibitors of metalloproteinases (TIMPs) may play an important role. The study presented herein was designed as a first demonstration of the regulative effects of CNP on MMPs/TIMPs expression in unilateral ureteral obstruction (UUO) rats. The continuous changes of CNP, MMP-2, MMP-9, TIMP-1, TIMP-2 and type IV collagen (Col-IV) expression were determined in the obstructed rat kidneys at 3 days, 1, 2, and 3 months post-UUO respectively. According to the real-time PCR analysis, CNP, MMP-2 and MMP-9 mRNA expression in the obstructed kidneys were significantly higher compared to every time corresponding SOR, and progressively decreased over time. In contrast, in the obstructed kidneys collected 2 and 3 months post-UUO, the higher TIMP-1 and TIMP-2 mRNA expression were observed in comparison to the corresponding SOR group. The above trends of CNP, MMP-2, MMP-9, TIMP-1, and TIMP-2 transcripts were confirmed by their protein expression based on immunohistochemistry and western blot, and finally contributed to the progressive elevated Col-IV expression in the obstructed kidneys throughout the entire study period. Overexpressed CNP may be an early compensatory response to counteract extracellular matrix remodeling in UUO rats.
虽然 C 型利钠肽(CNP)有益作用的机制尚未完全阐明,但调节基质金属蛋白酶(MMPs)/金属蛋白酶组织抑制剂(TIMPs)的表达可能起着重要作用。本研究旨在首次证明 CNP 对单侧输尿管梗阻(UUO)大鼠 MMPs/TIMPs 表达的调节作用。在 UUO 后 3 天、1 个月、2 个月和 3 个月,分别测定梗阻大鼠肾脏中 CNP、MMP-2、MMP-9、TIMP-1、TIMP-2 和 IV 型胶原(Col-IV)表达的连续变化。根据实时 PCR 分析,梗阻肾脏中的 CNP、MMP-2 和 MMP-9 mRNA 表达明显高于每个相应 SOR,并且随时间逐渐降低。相比之下,在 UUO 后 2 个月和 3 个月收集的梗阻肾脏中,与相应的 SOR 组相比,观察到更高的 TIMP-1 和 TIMP-2 mRNA 表达。根据免疫组织化学和 Western blot,CNP、MMP-2、MMP-9、TIMP-1 和 TIMP-2 转录物的上述趋势得到了证实,并最终导致在整个研究期间梗阻肾脏中 Col-IV 表达的逐渐升高。过表达的 CNP 可能是 UUO 大鼠对抗细胞外基质重塑的早期代偿反应。
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