Prostaglandin E2 receptor subtype 3?siRNA reduces the mesangial cell damage induced by TGF ?β1 through inhibiting MAPK pathway in mice
10.3760/cma.j.issn.1001-7097.2015.09.009
- VernacularTitle:前列腺素E2受体3亚型siRNA通过抑制MAPK信号通路减轻TGF-β1诱导的小鼠系膜细胞损伤
- Author:
Wen MA
;
Xiaolan CHEN
;
Yuyin XU
;
Fei LU
;
Yaping FAN
- Publication Type:Journal Article
- Keywords:
Receptors;
prostaglandin E;
RNA;
small interfering;
Transforming growth factor beta1;
Mesangial cells;
Cell proliferation;
MAP kinase signaling system
- From:
Chinese Journal of Nephrology
2015;31(9):686-692
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the effects and mechanisms of prostaglandin E2 receptor subtype 3 (EP3) on transforming growth factor β1 (TGF-β1)-induced mouse mesangial cells damage. Methods Primary mouse mesangial cells were separated and cultured. Three siRNAs were synthesized and transfected into mesangial cells for silencing EP3 by LipofectamineTM 2000 and the best one was chosen. MCs were grouped into: (1)control group; (2)TGF-β1 (10 μg/L) group; (3)NC-siRNA plus TGF-β1 (10 μg/L) group; (4) EP3-siRNA group; (5)EP3-siRNA plus TGF-β1 (10 μg/L). Then the proliferation of MCs was evaluated by CCK-8 assay. The expression of PGE2 and cAMP in cell supernatant were detected by ELISA. The mRNA and protein expression of fibronectin (FN), connective tissue growth factor (CTGF), cyclooxygenase-2 (COX2), membrane-bound prostaglandin E2 synthase 1 (mPGES1) were detected by real - time quantitative PCR and Western blotting. The phosphorylation of p38 MAPK and ERK1/2 was decected by Western blotting. Results Compared with control group, the cell proliferation induced by TGF-β1 was increased (P<0.05), the expression of PGE2 and cAMP were improved, mRNA and protein expression of FN, CTGF, COX2 and mPGES1 were up-regulated (all P<0.05). Compared with TGF-β1 group, the cell proliferation in EP3-siRNA plus TGF-β1 group was reduced, the expression of FN, CTGF, COX2 and mPGES1 mRNA and protein were downregulated (all P<0.05), the phosphorylation of ERK1/2, p38 MAPK were also declined (P<0.05). Conclusion EP3-siRNA may reduce TGF-β1-induced cell damage through upregulating the expression of cAMP, repressing the activity of ERK1/2 and p38 MAPK, inhibiting the expression of COX2 mPGES1 and PGE2 by feedback, then decreased the expression of FN and CTGF.
