胆汁淤积性微环境中甘氨鹅脱氧胆酸钠促进肝脏干细胞凋亡

李志鹏 王健 肖程 康权 罗庆

解剖学报 ›› 2019, Vol. 50 ›› Issue (6) : 747-753.

PDF(507 KB)
欢迎访问《解剖学报》官方网站!今天是 English
PDF(507 KB)
解剖学报 ›› 2019, Vol. 50 ›› Issue (6) : 747-753. DOI: 10.16098/j.issn.0529-1356.2019.06.008
细胞和分子生物学

胆汁淤积性微环境中甘氨鹅脱氧胆酸钠促进肝脏干细胞凋亡

  • 李志鹏1,2 王健1,2 肖程1,2 康权1* 罗庆2
作者信息 +

Effect of sodium glycosaminodeoxycholate on apoptosis of hepatic stem cells in cholestatic microenvironment

  • LI Zhi-peng 1,2 WANG Jian 1,2 XIAO Cheng 1,2 KANG Quan 1* LUO Qing2
Author information +
文章历史 +

摘要

目的 探讨在胆汁淤积性肝硬化病理微环境下对肝脏干细胞存活率的影响及体外甘氨鹅脱氧胆酸钠(GCDC)对肝脏干细胞凋亡的影响。 方法 以Balb/c小鼠胆总管结扎模型模拟胆汁淤积性肝硬化的病理环境并回输肝脏干细胞HP14-19,检测细胞定植存活情况;通过细胞计数试剂盒8(CCK-8)、结晶紫染色检测甘氨鹅脱氧胆酸钠对增殖的影响,流式细胞术检测细胞凋亡,通过Western blotting检测凋亡标志物Bax、Bcl-2、Caspase-3表达和磷酸化腺嘌呤核苷二磷酸依赖性蛋白激酶α(p-AMPKα)、腺嘌呤核苷二磷酸依赖性蛋白激酶α(AMPKα)等的表达。 结果 通过CCK-8检测和结晶紫染色发现,随着甘氨鹅脱氧胆酸钠作用浓度的增加,HP14-19细胞的增殖抑制;流式细胞术提示,GCDC处理组细胞凋亡率明显增加(P<0.05);Western blotting检测发现,与对照组相比,实验组凋亡基因Bax、Caspase-3蛋白表达上调,抗凋亡基因Bcl-2蛋白表达下调,AMPKα活化增加(P<0.05)。 结论 胆汁淤积性肝硬化所导致的胆汁淤积微环境诱导肝脏干细胞发生凋亡。

Abstract

Objective To investigate the effects of hepatic stem cells survival in the pathological microenvironment of cholestatic cirrhosis, and the effects of sodium glycosaminodeoxycholate (GCDC) on apoptosis of hepatic stem cells in vitro. Methods Balb/c mice were subjected to bile duct ligation (BDL)to simulate the pathological environment of cholestatic cirrhosis;Liver stem cells HP14-19 were transplanted back into liver by the splenic vein and survival of cell colonization was detected;Effects of sodium glycosaminodeoxycholate on the viability of HP14-19 cells at different concentrations by cell counting kit-8(CCK-8) and crystal violet staining, flow cytometry was used to detect the apoptosis of HP14-19 cells treated with 600 μmol/L GCDC 24 hours later, and the expression of Bax,Bcl-2,Capase-3,phosphorylated adenosine 5’-monophosphate-activated protein kinase α(p-AMPKα) and adenosine 5’-monophosphate-activated protein kinase α(AMPKα) were detected by Western blotting. Results The results of CCK-8 and crystal violet staining showed that the proliferation of HP14-19 cells was inhibited with the increase of the concentration of sodium glycosaminodeoxycholate. Flow cytometry showed that the apoptosis rate of GCDC treated group was higher than that of control group. Compared with the control group, the expression of Bax, Capase-3 was up-regulated and the expression of Bcl-2 protein was down-regulated in the experimental group. The results showed that GCDC could induce apoptosis of HP14-19 (P<0.05) AMPK was activated. Conclusion Microenvironment of cholestatic cirrhosis induced apoptosis of liver stem cells.

关键词

胆汁淤积性肝硬化 / 甘氨鹅脱氧胆酸钠 / 肝脏干细胞 / 免疫印迹法 / 小鼠

Key words

Cholestatic cirrhosis / Sodium glycosaminodeoxycholate / Liver stem cell / Western blotting / Mouse

引用本文

导出引用
李志鹏 王健 肖程 康权 罗庆. 胆汁淤积性微环境中甘氨鹅脱氧胆酸钠促进肝脏干细胞凋亡[J]. 解剖学报. 2019, 50(6): 747-753 https://doi.org/10.16098/j.issn.0529-1356.2019.06.008
LI Zhi-peng WANG Jian XIAO Cheng KANG Quan LUO Qing. Effect of sodium glycosaminodeoxycholate on apoptosis of hepatic stem cells in cholestatic microenvironment[J]. Acta Anatomica Sinica. 2019, 50(6): 747-753 https://doi.org/10.16098/j.issn.0529-1356.2019.06.008

参考文献

 [1]  Xiang B,Xie XL. Sequential treatment of “Kasai surgery-liver transplantation” for biliary atresia [J].Journal of Clinical Pediatric Surgery, 2018 17(11): 805-808. (in Chinese)
向波, 谢小龙. 胆道闭锁的“Kasai手术-肝移植”序贯治疗[J]. 临床小儿外科杂志, 2018,17(11):805-808.
 [2] LeeVan E, Matsuoka L, Cao S, et al. Biliary-enteric drainage vs primary liver transplant as initial treatment for children with biliary atresia[J]. JAMA Surg, 2019,154(1):26-32.
 [3] Zhang YJ, Li YY, Hao XN,et al.Vein transplantation of human umbilical cord-derived mesenchymal stem cells for treatment of hepatic fibrosis in rats[J].Chinese Journal of Tissue Engineering Research, 2014, 18(28): 4485-4490. (in Chinese)
张英杰, 李玉云, 郝晓娜, 等. 人脐带源间充质干细胞静脉移植治疗大鼠肝纤维化[J]. 中国组织工程研究, 2014,18(28):4485-4490.
 [4] Guo CC, Lan L, Liu R,et al. Co-transplantation of endothelial progenitor cells and hepatocyte stem cells launches a counterattack against liver fibrosis in rats [J].Chinese Journal of Tissue Engineering Research, 2018, 22(5): 704-709. (in Chinese)
郭灿灿, 兰玲, 刘冉, 等. 内皮祖细胞和肝干细胞联合移植对大鼠肝纤维化的逆转作用[J]. 中国组织工程研究, 2018,22(05):704-709.
 [5] Bria A, Marda J, Zhou J, et al. Hepatic progenitor cell activation in liver repair[J]. Liver Res, 2017,1(2):81-87.
 [6] Zhao MX,Li BW,Wang DSh, et al. Role of miR-122 in bone marrow derived stem cell therapy for acute liver injury in rats[J].Journal of Jilin University(Medicine Edition), 2015,41(6):1150-1153.  (in Chinese)
赵民学, 李柏文, 王德盛, 等. miR-122在骨髓间充质干细胞治疗大鼠急性肝损伤中的作用[J]. 吉林大学学报(医学版), 2015,41(6):1150-1153.
 [7] Bi Y, He Y, Huang J, et al. Functional characteristics of reversibly immortalized hepatic progenitor cells derived from mouse embryonic liver[J]. Cell Physiol Biochem, 2014,34(4):1318-1338.
 [8] éboli L, Tannuri AC, Gibelli N, et al. Comparison of the results of living donor liver transplantation due to acute liver failure and biliary atresia in a quaternary center[J]. Transplant Proc, 2017,49(4):832-835.
 [9] Namdaroglu S, Kaya AH, Batgi H, et al. Impacts of post-transplantation cyclophosphamide treatment after allogeneic hematopoietic stem cell transplantation in acute myeloid leukemia[J]. Sci Rep, 2019,9(1):2046.
 [10] Warren CFA, Wong-Brown MW, Bowden NA. BCL-2 family isoforms in apoptosis and cancer[J]. Cell Death Dis, 2019,10(3):177.
 [11] Tan KO, Fu NY, Sukumaran SK, et al. MAP-1 is a mitochondrial effector of Bax[J]. Proc Natl Acad Sci USA, 2005,102(41):14623-14628.
 [12] Shi Y. Mechanisms of caspase activation and inhibition during apoptosis[J]. Mol Cell, 2002,9(3):459-470.
 [13] Zhang JF,Zhao ZhH,Hao JH,et al.Effects of microRNA-25 on cerebral ischemia/reperfusion injury-induced cell apoptosis[J]. Acta Anatomica Sinica, 2018,49(5):584-590.  (in Chinese)
张军峰, 赵朝华, 郝佳晖, 等. MicroRNA-25在脑缺血/再灌注损伤诱导的细胞凋亡过程中的作用[J]. 解剖学报, 2018,49(5):584-590.
 [14] Xiao J,Yin SM,Xie ShF,et al.Quercetin modulate AMPK activity and induce apoptosis and autophagy in HL-60 cells[J].Journal of Sun Yat-Sen University(Medical Sciences), 2018,39(4):501-509.  (in Chinese)
肖洁, 尹松梅, 谢双锋, 等. 槲皮素调控AMPK活性诱导HL-60细胞自噬与凋亡[J]. 中山大学学报(医学科学版), 2018,39(4):501-509.
 [15] Zhu Y, Wang Q, Tang X, et al. Mesenchymal stem cells enhance autophagy of human intrahepatic biliary epithelial cells in vitro[J]. Cell Biochem Funct, 2018,36(5):280-287.
 [16] Gao L, Lv G, Guo X, et al. Activation of autophagy protects against cholestasis-induced hepatic injury[J]. Cell Biosci, 2014,4:47.
 [17] Yang B, Luo Q, Kang Q,et al. Tumor necrosis factor-α and transforming growth factor-β1 balance liver stem cell differentiation in cholestatic cirrhosis[J] Journal of Southern Medical University, 2018, 38(4): 375-383.  (in Chinese)
杨博, 罗庆, 康权, 等. TNF-α、TGF-β-1在胆汁淤积性肝硬化中平衡调控肝脏干细胞分化[J]. 南方医科大学学报, 2018,38(4):375-383.
 [18] Sun X, Zhang W. Silencing of Gal-7 inhibits TGF-β1-induced apoptosis of human airway epithelial cells through JNK signaling pathway[J]. Exp Cell Res, 2019,375(2):100-1010.
 [19] Park S, In Hwang S, Kim J, et al. The therapeutic potential of induced hepatocyte-like cells generated by direct reprogramming on hepatic fibrosis[J]. Stem Cell Res Ther, 2019,10(1):21.
 [20] Hu C, Zhao L, Duan J, et al. Strategies to improve the efficiency of mesenchymal stem cell transplantation for reversal of liver fibrosis[J]. J Cell Mol Med, 2019,23(3):1657-1670.
 [21] Hohenester S, Vennegeerts T, Wagner M, et al. Physiological hypoxia prevents bile salt-induced apoptosis in human and rat hepatocytes[J]. Liver Int, 2014,34(8):1224-1231.

基金

分化抑制因子(Id)在骨髓间充质干细胞成骨异常分化于骨肉瘤形成的调控研究

PDF(507 KB)

Accesses

Citation

Detail

段落导航
相关文章

/