Tianjin Medical Journal ›› 2019, Vol. 47 ›› Issue (3): 230-234.doi: 10.11958/20181295
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CHEN Xiang,HUANG Ying,LONG Chun-yi,LIAO Pin-hu
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CHEN Xiang, HUANG Ying, LONG Chun-yi, LIAO Pin-hu. miR-21 regulates PTEN/AKT pathway to affect the expression of MMP-2 and MMP-9 in podocytes induced by LPS[J]. Tianjin Medical Journal, 2019, 47(3): 230-234.
Abstract: Objective To study the effects and the regulation mechanism of microRNA-21 (miRNA-21, miR-21) on the expressions of matrix metalloproteinase 2 (MMP-2) and MMP-9 in podocytes under lipid polysaccharide (LPS) stimulation in phosphatase and tensin homology deleted on chromosome ten (PTEN) / phosphorylated protein kinase B (pAKT) signaling pathway. Methods The podocytes of 3-8 generation were divided into LPS group and control group. LPS group was given 10 mg/L LPS. The control group was given the same dose of phosphate buffer saline. After 24 h, expressions of miR-21, MMP-2 and MMP-9 were detected by real-time fluorescent quantitative PCR and ELISA, and the correlation between miR-21, MMP-2 and MMP-9 was analyzed. The model of podocyte injury interfered by exogenous miR-21 under LPS stimulation was constructed. The effects of exogenous miR-21 on expressions of MMP-2, MMP-9, PTEN and p-AKT were detected by Western blot assay. Results Compared with the control group, the expressions of miR-21, MMP-2 and MMP-9 increased in podocytes under LPS stimulation, and they were positively correlated (P<0.05). After the expression of exogenous miR-21 was up-regulated, the expressions of MMP-2, MMP-9 and p-AKT increased but the expression of PTEN decreased (P<0.05). While the expression of exogenous miR-21 was controlled, the expressions of MMP-2, MMP-9 and pAKT decreased but the expression of PTEN increased (P<0.05). Conclusion The miR-21 can regulate PTEN / AKT pathway to affect the expressions of MMP-2 and MMP-9 under LPS stimulation in podocytes.
Key words: microRNAs, matrix metalloproteinase 2, matrix metalloproteinase 9, PTEN phosphohydrolase, oncogene protein v-akt, podocytes, microRNA-21
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URL: https://www.tjyybjb.ac.cn/EN/10.11958/20181295
https://www.tjyybjb.ac.cn/EN/Y2019/V47/I3/230