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本文引用的文献

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Exp Ther Med. 2015 Jul;10(1):106-112. doi: 10.3892/etm.2015.2468. Epub 2015 Apr 30.
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New approaches to selectively target cancer-associated matrix metalloproteinase activity.选择性靶向与癌症相关的基质金属蛋白酶活性的新方法。
Cancer Metastasis Rev. 2014 Dec;33(4):1043-57. doi: 10.1007/s10555-014-9530-4.
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Matrix metalloproteinases as biomarkers of disease: updates and new insights.基质金属蛋白酶作为疾病的生物标志物:最新进展和新见解。
Clin Chem Lab Med. 2015 Feb;53(3):349-55. doi: 10.1515/cclm-2014-0520.
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Ramipril inhibits AGE-RAGE-induced matrix metalloproteinase-2 activation in experimental diabetic nephropathy.雷米普利抑制 AGE-RAGE 诱导的实验性糖尿病肾病中基质金属蛋白酶-2 的激活。
Diabetol Metab Syndr. 2014 Aug 13;6(1):86. doi: 10.1186/1758-5996-6-86. eCollection 2014.
5
Tribbles 3 regulates the fibrosis cytokine TGF- β 1 through ERK1/2-MAPK signaling pathway in diabetic nephropathy.Tribbles 3 通过 ERK1/2-MAPK 信号通路调节糖尿病肾病纤维化细胞因子 TGF-β1。
J Immunol Res. 2014;2014:240396. doi: 10.1155/2014/240396. Epub 2014 Jul 16.
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Diabetic nephropathy--emerging epigenetic mechanisms.糖尿病肾病——新兴的表观遗传机制。
Nat Rev Nephrol. 2014 Sep;10(9):517-30. doi: 10.1038/nrneph.2014.116. Epub 2014 Jul 8.
7
Myeloperoxidase deficiency ameliorates progression of chronic kidney disease in mice.髓过氧化物酶缺乏症可改善小鼠慢性肾脏病的进展。
Am J Physiol Renal Physiol. 2014 Aug 15;307(4):F407-17. doi: 10.1152/ajprenal.00262.2014. Epub 2014 Jul 2.
8
Imbalance between MMP-2, 9 and TIMP-1 promote the invasion and metastasis of renal cell carcinoma via SKP2 signaling pathways.基质金属蛋白酶-2、9与金属蛋白酶组织抑制因子-1之间的失衡通过SKP2信号通路促进肾细胞癌的侵袭和转移。
Tumour Biol. 2014 Oct;35(10):9807-13. doi: 10.1007/s13277-014-2256-7. Epub 2014 Jul 2.
9
Effects of high glucose on integrin activity and fibronectin matrix assembly by mesangial cells.高糖对系膜细胞整合素活性及纤连蛋白基质组装的影响。
Mol Biol Cell. 2014 Aug 15;25(16):2342-50. doi: 10.1091/mbc.E14-03-0800. Epub 2014 Jun 18.
10
Matrix metalloproteinase-9 deficiency attenuates diabetic nephropathy by modulation of podocyte functions and dedifferentiation.基质金属蛋白酶-9 缺乏通过调节足细胞功能和去分化来减轻糖尿病肾病。
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C肽对高糖刺激的大鼠系膜细胞中的基质金属蛋白酶-9具有晚期诱导作用。

C-peptide exhibits a late induction effect on matrix metallopeptidase-9 in high glucose-stimulated rat mesangial cells.

作者信息

Wang Junxia, Li Yanning, Xu Mingzhi, Li Dandan, Wang Yu, Qi Jinsheng, He Kunyu

机构信息

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.

出版信息

Exp Ther Med. 2016 Dec;12(6):4142-4146. doi: 10.3892/etm.2016.3873. Epub 2016 Nov 4.

DOI:10.3892/etm.2016.3873
PMID:28101192
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5228027/
Abstract

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.

摘要

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。