Chinese Journal of Nephrology, Dialysis & Transplantation ›› 2016, Vol. 25 ›› Issue (6): 533-538.DOI: 10.3969/cndt.j.issn.1006-298X.2016.06.006
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Abstract:
Objective:To explore the potential role and mechanism of microRNA497 in the glomerular mesangial cell pyroptosis induced by high glucose and insulin. Methodology:High glucose and insulin was used to treat human renal mesangial cells (HRMC). At various time points, cell pyroptosis was detected with flow cytometry, and realtime qPCR was used to detect miR497 levels in HRMC. Then, various concentrations of miR497 mimic were transfected to HRMC. The mRNA levels of key genes in pyroptotic pathway, including IL1β, TNFα and caspase1 were detected. Bioinformatics and Luciferase Reporter Gene assay were used to predict and verify the target of miR497 to nucleotidebinding oligomerization domain receptor P1 (NLRP1) inflammasome. The miR497 mimic and pcDNANLRP1 expression vector were transfected individually or cotransfected to HRMC. Western blotting was used to detect the levels of NLRP1 protein, and cell pyroptosis were detected. Results:HRMC treated with high glucose and insulin for more than 48h, HRMC pyroptosis was significantly increased, and the expression level of miR497 was decreased (P<005). After transfected with miR497 mimic, the pyroptosis of HRMC was significantly ameliorated, and the mRNA expression of IL1β, TNFα and caspase1 were downregulated (P<005). miR497 directly targeted at NLRP1 gene and suppressed NLRP1 protein expression. NLRP1 overexpression completely rescued the inhibition of cell pyroptosis caused by miR497. Conclusion:The HRMC pyroptosis was suppressed miR497, and inflammation response was induced by high glucose and insulin.
Key words: pyroptosis, high glucose and insulin, microRNA-497, NLRP1 inflammasome, caspase1
LI Rong,ZHENG Haolin,TIAN Xiujuan, et al. Potential role and mechanism of microRNA-497 in the glomerular mesangial cell pyroptosis[J]. Chinese Journal of Nephrology, Dialysis & Transplantation, 2016, 25(6): 533-538.
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URL: http://www.njcndt.com/EN/10.3969/cndt.j.issn.1006-298X.2016.06.006
http://www.njcndt.com/EN/Y2016/V25/I6/533