Propofol suppresses adipose-derived stem cell progression via PI3K/AKT-Wnt signaling pathway

被引:1
|
作者
Yin, Guoping [1 ]
Wang, Jia [1 ]
Zhong, Yanling [1 ]
Wu, Weidong [2 ,3 ]
机构
[1] Nanjing Univ Chinese Med, Hosp Nanjing 2, Dept Anesthesiol, Nanjing 210003, Peoples R China
[2] Nantong Univ, Dept Anesthesiol, Danyang Peoples Hosp Jiangsu Prov, Danyang 212300, Jiangsu, Peoples R China
[3] Nantong Univ, Danyang Hosp, Danyang 212300, Jiangsu, Peoples R China
关键词
Adipose-derived stem cells; Propofol; Proliferation; PI3K; AKT-Wnt; BONE;
D O I
10.1186/s12871-022-01603-x
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Adipose-derived stem cell (ADSC) transplantation has become a prospective way to treat cardiovascular diseases and skin traumas. Propofol, a short-acting intravenous anesthetic agent, plays an important role in the induction and maintenance of general anesthesia. In this study, we investigated the effects of propofol on ADSCs. The flow cytometry results showed that ADSCs were positive for CD29, CD44, and CD90 and negative for CD31, CD34, and CD45. The results of MTT and BrdU assays demonstrated that propofol impeded the proliferation of ADSCs. The cell scratch test showed that propofol had an inhibitory effect on the migration of ADSCs. Transwell assay showed that invasive ASDC counts decreased significantly after propofol treatment. Propofol also promoted ADSC apoptosis and arrested ADSCs in the G0/G1 phase. All these effects showed in a dose-dependent manner that the higher the concentration, the stronger the effect. Western blot analysis revealed decreased levels of FAK, PI3K, AKT, and GSK3 beta phosphorylation, while the phosphorylation of beta-catenin increased after 48 h of treatment with propofol. The findings above indicated that the PI3K/AKT-Wnt pathways mediated propofol-inhibited ADSC proliferation, providing new insights into the propofol application in ADSCs.
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页数:11
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