Delphinidin protects β2m-/Thy1+bone marrow-derived hepatocyte stem cells against TGF-β1-induced oxidative stress and apoptosis through the PI3K/Akt pathway in vitro

被引:15
作者
Chen, Jiang [1 ]
Li, Hong-Yu [1 ]
Wang, Di [1 ]
Guo, Xiao-Zhong [1 ]
机构
[1] Shenyang Gen Hosp PLA, Dept Gastroenterol, 83 Wenhua Rd, Shenyang 110016, Liaoning, Peoples R China
关键词
Delphinidin; beta 2m-/Thy1+stem cells; TGF-beta; 1; Apoptosis; Oxidative stress; PI3K/Akt; GROWTH-FACTOR-BETA; LIVER FIBROSIS; TRANSPLANTATION; INVOLVEMENT; HEPATITIS; EXTRACT; DEATH;
D O I
10.1016/j.cbi.2018.10.019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
beta 2m-/Thy2+ bone marrow-derived hepatocyte stem cells (BDHSCs) have a potential to be applied for cellular treatment in liver cirrhosis. However, the resultant tissue regeneration is restricted by transplanted cells death. The accumulation of transforming growth factor beta 1 (TGF-beta 1) in liver fibrosis local microenvironment may play an essential role in the rapid cell death of implanted beta 2m-/Thy1+ BDHSCs. The main mechanism of poor survival of the target stem cells is still unknown. Delphinidin, an anthocyanidin, has potent antioxidant and anti-inflammatory activities. However, whether this bio-active ingredient can substantially contribute to beta 2m-/Thy1+ BDHSCs' protection from TGF-beta 1 induced apoptosis in vitro remains to be elucidated. In the present research, we determined whether delphinidin pretreatment can improve the survival of beta 2m-/Thy1+ BDHSCs during exposure to TGF-beta 1 and elucidated its underlying mechanisms. By using TGF-beta 1, we induced the apoptosis of beta 2m-/Thy1+ BDHSCs and assessed the apoptotic rates up to 24 h by flow cytometry. beta 2m-/Thy1+ BDHSC proliferation was gauged using 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyl- 2H-tetrazolium bromide (MIT) assay. The expression grades of Bc1-2, Akt, caspase-3, and Box were observed through Western blot analysis. We found that delphinidin can significantly impede TGF-beta 1-induced apoptosis dose-dependently, scavenge reactive oxygen species (ROS), and inhibit the discharge of caspase-3 in beta 2m-/Thy1+ BDHSCs. We also demonstrated that delphinidin can activate the phosphatidylinosito1-3-kinase (PI3K)/Akt signaling pathway. The suppression of ROS and succeeding apoptosis was achieved by pretreatment with LY294002, a PI3K/Akt pathway inhibitor. In summary, our findings revealed that delphinidin can protect beta 2m-/Thy1+ BDHSCs from apoptosis and ROS-dependent oxidative stress induced by the TGF-beta 1 via PI3K/Akt signaling pathway. On the basis of these data, delphinidin can be regarded as a promising anti-apoptotic agent for enhancing beta 2m-/Thy1+ BDHSC survival during cell transplantation in liver cirrhosis patients.
引用
收藏
页码:109 / 118
页数:10
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