Effect on M1 macrophages of shenlian extracts.
- Author:
Bing-Bing ZHOU
;
Yu-Jie LI
;
Qi LI
;
Qing YANG
;
Xiao-Gang WENG
;
Ying CHEN
;
Ya-Jie WANG
;
Xiao-Xin ZHU
- Publication Type:Journal Article
- MeSH:
Animals;
Cell Line;
Cell Shape;
drug effects;
Cell Survival;
drug effects;
Drugs, Chinese Herbal;
pharmacology;
Interferon-gamma;
genetics;
immunology;
Interleukin-6;
genetics;
immunology;
Macrophages;
cytology;
drug effects;
immunology;
Mice;
Tumor Necrosis Factor-alpha;
genetics;
immunology
- From:
China Journal of Chinese Materia Medica
2014;39(11):2086-2090
- CountryChina
- Language:Chinese
-
Abstract:
This study discusses the effects of Shenlian extracts (SL) on M1 macrophages in atherosclerosis. The MTT assay was used to detect the growth inhibition rates of RAW264.7 cells. RAW264.7 cells were stimulated with murine interferon-gamma (IFN-gamma) plus lipopolysaccharide (LPS) to induce M1 macrophages. The different concentrations of SL extracts (high-dose 50 mg x L(-1), moderate-dose 25 mg x L(-1), low-dose 12.5 mg x L(-1)) were added. The CD86 of M1 macrophages in cell membrane was measured by flow cytometry. The mRNA expression of iNOS and TNF-alpha gene was detected by reverse transcription PCR (RT-PCR). And the supernatants were collected, the content of IL-6 and TNF-alpha were detected with ELISA kits. The results of this experiment show that the expression of the cell membrane molecule CD86, iNOS and TNF-alpha gene, the content of IL-6 and TNF-alpha was obviously increased in M1 macrophages by IFN-gamma and LPS. The different doses of SL extract could reduce the expression of the above indicators. The above experimental results demonstrate that IFN-gamma combined LPS can induce RAW264.7 cell to type into M1 macrophages, and SL extracts can inhibit M1 macrophages.
