自噬
脂肪生成
间充质干细胞
PI3K/AKT/mTOR通路
细胞凋亡
骨髓
细胞生长
再生障碍性贫血
细胞周期
癌症研究
化学
流式细胞术
细胞
细胞生物学
生物
免疫学
生物化学
作者
Xin Wang,Fengxia Ma,Shihong Lu,Ying Chi,Fang Chen,Xue Li,Juanjuan Li,Wenjing Du,Ying Feng,Junjie Cui,Baoquan Song,Zhongchao Han
出处
期刊:PubMed
日期:2014-06-01
卷期号:22 (3): 762-6
被引量:5
标识
DOI:10.7534/j.issn.1009-2137.2014.03.035
摘要
This study was aimed to investigate the effects of rapamycin on biological function and autophagy of bone marrow mesenchymal stem cells (BM-MSC) from patients with aplastic anemia so as to provide experimental basis for the clinical treatment of aplastic anemia (AA) with rapamycin. BM-MSC were treated with different concentrations of rapamycin (0, 10, 50, 100 nmol/L) for 48 h, the expression of LC3B protein was detected by Western blot to observe the effect of rapamycin on cell autophagy; cell apoptosis and cell cycles were detected by flow cytometry; the proliferation of BM-MSC of AA patients was measured by cell counting kit-8; the adipogenic differentiation of BM-MSC were tested by oil red O staining after adipogenic induction for 2 weeks; the adipogenic related genes (LPL, CFD, PPARγ) were detected by real-time PCR. The results showed that the proliferation and adipogenesis of BM-MSC of AA patients were inhibited by rapamycin. Moreover, the autophagy and apoptosis of BM-MSC were increased by rapamycin in a dose-dependent way.Rapamycin arrested the BM-MSC in G0/G1 phase and prevented them into S phase (P < 0.05). It is concluded that rapamycin plays an critical role in inhibiting cell proliferation, cell cycles, and adipogenesis, these effects may be related with the autophagy activation and mTOR inhibition resulting from rapamycin.
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