Wang Junxia, Li Yanning, Xu Mingzhi, Li Dandan, Wang Yu, Qi Jinsheng, He Kunyu
Department of Molecular Biology, Hebei Key Lab of Laboratory Animal Science, Hebei Medical University, Shijiazhuang, Hebei 050017, P.R. China.
Department of Biochemistry, Hebei Key Laboratory of Medical Biotechnology, Hebei Medical University, Shijiazhuang, Hebei 050017, P.R. China.
Exp Ther Med. 2016 Dec;12(6):4142-4146. doi: 10.3892/etm.2016.3873. Epub 2016 Nov 4.
Insufficient matrix metalloproteinase (MMP)-9 and MMP-2 is considered to be a contributor of extracellular matrix (ECM) accumulation in diabetic nephropathy (DN). C-peptide can reverse fibrosis, thus exerting a beneficial effect on DN. Whether C-peptide induces MMP-9 and MMP-2 to reverse ECM accumulation is not clear. In the present study, in order to determine ECM metabolism, rat mesangial cells were treated with high glucose (HG) and C-peptide intervention, then the early and late effects of C-peptide on HG-affected MMP-9 and MMP-2 were evaluated. Firstly, it was confirmed that HG mainly suppressed MMP-9 expression levels. Furthermore, C-peptide treatment induced MMP-9 expression at 6 h and suppressed it at 24 h, revealing the early dual effects of C-peptide on MMP-9 expression. Subsequently, significant increase in MMP-9 expression at 72, 96 and 120 h C-peptide treatment was observed. These changes in MMP-9 protein content confirmed its expression changes following late C-peptide treatment. Furthermore, at 96 and 120 h C-peptide treatment reversed the HG-inhibited MMP-9 secretion, further indicating the late induction effect of C-peptide on MMP-9. The present results demonstrated that C-peptide exerted a late induction effect on MMP-9 in HG-stimulated rat mesangial cells, which may be associated with the underlying mechanism of C-peptide's reversal effects on DN.
基质金属蛋白酶(MMP)-9和MMP-2不足被认为是糖尿病肾病(DN)细胞外基质(ECM)积聚的一个促成因素。C肽可以逆转纤维化,从而对DN产生有益作用。C肽是否通过诱导MMP-9和MMP-2来逆转ECM积聚尚不清楚。在本研究中,为了确定ECM代谢情况,用高糖(HG)处理大鼠系膜细胞并进行C肽干预,然后评估C肽对受HG影响的MMP-9和MMP-2的早期和晚期作用。首先,证实HG主要抑制MMP-9的表达水平。此外,C肽处理在6小时时诱导MMP-9表达,而在24小时时抑制其表达,揭示了C肽对MMP-9表达的早期双重作用。随后,观察到在C肽处理72、96和120小时时MMP-9表达显著增加。MMP-9蛋白含量的这些变化证实了C肽后期处理后其表达的变化。此外,在C肽处理96和120小时时逆转了HG抑制的MMP-9分泌,进一步表明C肽对MMP-9的后期诱导作用。本研究结果表明,C肽对HG刺激的大鼠系膜细胞中的MMP-9发挥后期诱导作用,这可能与C肽对DN的逆转作用的潜在机制有关。