The Expression of TLR2 mRNA in Rat Peritoneal Mesothelial Cells Stimulated by Lipopolysaccharide,Rosiglitazone and Highglucose
Lining Wang
Abstract
Lining Wang
Abstract
Objective To observe the effect of rosiglitazone on the mRNA expression of toll-like receptor 2 in rat peritoneal mesothelial cell (RPMC) stimulated by Lipopolysaccharide(LPS) and to observe the expression of toll-like receptor 2 in RPMC stimulated by highglucose. Methods RPMC were isolated from rat colic omentum and were incubated with LPS (1.0 μg/ml,10 μg/ml,100 μg/ml),or stimulated by Rosiglitazone(10 μmol/L) after incubated with LPS (10 μg/ml) for 2 h. The RPMC were under the stimulation of highglucose (1.5%,2.5%,4.25%). RPMC in the control group were just incubated with medium. TLR2 mRNA was detected by RT-PCR. Results Compared with the control group,the expression of TLR2 mRNA was significantly increased in the groups stimulated by LPS and highglucose. In the group pre-incubated with LPS,compared with the group stimulated by LPS,the up-regulating expression of TLR2 mRNA was significantly inhibited. Conclusion LPS and highglucose can up-regulate the expression of TLR2 mRNA in rat peritoneal mesothelial cell. Rosiglitazone can inhibit the up-regulating effect of LPS on the expression of TLR2 mRNA.
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Objective To observe the effect of rosiglitazone on the mRNA expression of toll-like receptor 2 in rat peritoneal mesothelial cell (RPMC) stimulated by Lipopolysaccharide(LPS) and to observe the expression of toll-like receptor 2 in RPMC stimulated by highglucose. Methods RPMC were isolated from rat colic omentum and were incubated with LPS (1.0 μg/ml,10 μg/ml,100 μg/ml),or stimulated by Rosiglitazone(10 μmol/L) after incubated with LPS (10 μg/ml) for 2 h. The RPMC were under the stimulation of highglucose (1.5%,2.5%,4.25%). RPMC in the control group were just incubated with medium. TLR2 mRNA was detected by RT-PCR. Results Compared with the control group,the expression of TLR2 mRNA was significantly increased in the groups stimulated by LPS and highglucose. In the group pre-incubated with LPS,compared with the group stimulated by LPS,the up-regulating expression of TLR2 mRNA was significantly inhibited. Conclusion LPS and highglucose can up-regulate the expression of TLR2 mRNA in rat peritoneal mesothelial cell. Rosiglitazone can inhibit the up-regulating effect of LPS on the expression of TLR2 mRNA.
Key concepts: TLR2, Lipopolysaccharide, Messenger RNA, Mesothelial Cell, Toll-like receptor, Stimulation, Receptor, Rosiglitazone