Effect of Angiotensin II and Angiotensin-(1-7) at Different Concentrations on Peroxisome Proliferator Activated Receptorγ Expression in THP-1 Macrophage
Kang Xiao
Abstract
Kang Xiao
Abstract
Aim To investigate the effect of angiotensinⅡ(AngⅡ),angiotensin-(1-7)(Ang(1-7)) at different concentrations on the expression of peroxisome proliferator activated receptorγ(PPARγ) in cultured human THP-1 macrophages. Methods Monocytic THP-1 cells were cultured with 100 nmol/L phorbol myristate acetate(PMA) for 48 hours to lead cells into THP-1 macrophage.Handle the cells in different conditions for 24 hours: medium added nothing,different concentration of Ang-(1-7)(0.1,1,10 μmol/L),different concentration of AngⅡ(0.1,1,5,10 μmol/L).mRNA and protein expression of PPARγ in THP-1 macrophages was measured by RT-PCR and Western Blotting respectively. Results Compared with control group,mRNA and protein expression of PPARγ were increased in Ang(1-7) groups,and they both expressed more as concentration of Ang(1-7) increasing(0.1,1,10 μmol/L).mRNA and protein expressions of PPARγ were decreased in AngⅡgroups compared with control group,and the mRNA and protein both expressed less as concentration of AngⅡ increasing(0.1,1,5,10 μmol/L)(P0.05). Conclusion Ang(1-7) can increase PPARγ expression in THP-1 macrophages in dose-dependent manners.AngⅡcan decrease PPARγ expression in dose-dependent manners.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Aim To investigate the effect of angiotensinⅡ(AngⅡ),angiotensin-(1-7)(Ang(1-7)) at different concentrations on the expression of peroxisome proliferator activated receptorγ(PPARγ) in cultured human THP-1 macrophages. Methods Monocytic THP-1 cells were cultured with 100 nmol/L phorbol myristate acetate(PMA) for 48 hours to lead cells into THP-1 macrophage.Handle the cells in different conditions for 24 hours: medium added nothing,different concentration of Ang-(1-7)(0.1,1,10 μmol/L),different concentration of AngⅡ(0.1,1,5,10 μmol/L).mRNA and protein expression of PPARγ in THP-1 macrophages was measured by RT-PCR and Western Blotting respectively. Results Compared with control group,mRNA and protein expression of PPARγ were increased in Ang(1-7) groups,and they both expressed more as concentration of Ang(1-7) increasing(0.1,1,10 μmol/L).mRNA and protein expressions of PPARγ were decreased in AngⅡgroups compared with control group,and the mRNA and protein both expressed less as concentration of AngⅡ increasing(0.1,1,5,10 μmol/L)(P0.05). Conclusion Ang(1-7) can increase PPARγ expression in THP-1 macrophages in dose-dependent manners.AngⅡcan decrease PPARγ expression in dose-dependent manners.
Key concepts: THP1 cell line, Peroxisome proliferator-activated receptor, Angiotensin II, Receptor, Messenger RNA, Endocrinology, Blot, Internal medicine