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Bile salts inhibit growth and induce apoptosis of culture human normal esophageal mucosal epithelial cells

机译:胆汁盐抑制人正常食管粘膜上皮细胞的生长并诱导其凋亡

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摘要

AIM: To investigate the effect of six bile salts: glycocholate (GC), glycochenodeoxycholate (GCDC), glycodeoxycholate (GDC), taurocholate (TC), taurochenodeoxycholate (TCDC), taurodeoxycholate (TDC), and their mixture on cultured human normal esophageal mucosal epithelial cells.METHODS: Human normal esophageal mucosal epithelial cells were cultured with serum-free keratinocyte medium. 3-[4,5-Dimethylthiaolyl]-2,5-diphenyl-tetrazolium bromide assay was applied to the detection of cell proliferation. Apoptotic morphology was observed by phase-contrast video microscopy and terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) assay. Sub-G1 DNA fragmentations and early apoptotic cells were assayed by flow cytometry (FCM) with propidium iodide (PI) staining and annexin V-FITC conjugated with PI staining. Apoptotic DNA ladders on agarose gel electrophoresis were observed.RESULTS: Except for GC, GCDC, GDC, TC, TCDC, TDC and their mixture could initiate growth inhibition of esophageal mucosal epithelial cells in a dose- and time-dependent manner. TUNEL and FCM assays demonstrated that the bile salts at 500 μmol/L and their mixture at 1 500 μmol/L induced apoptosis except for GC. The percentage of sub-G1 detected by FCM with PI staining was 83.5% in cells treated with 500 μmol/L TC for 2 h, and 19.8%, 20.4%, 25.6%, 13.5%, and 75.8% in cells treated with 500 μmol/L GCDC, TCDC, GDC, TDC, and 1 500 μmol/L mixture for 24 h, respectively, which were higher than that of the control (1.5%). The percentage was 1.4% in cells with 500 μmol/L GC for 24 h. DNA ladders on agarose gel electrophoresis were seen in cells treated with 500 μmol/L TC for 2 h and 1 500 μmol/L mixture for 24 h.CONCLUSION: All GCDC, GDC, TC, TCDC, TDC and their mixture can inhibit growth and induce apoptosis of cultured human normal esophageal mucosal epithelial cells, but GC is well tolerated by the cells.
机译:目的:研究六种胆汁盐:糖胆酸(GC),糖去氧胆酸(GCDC),糖脱氧胆酸(GDC),牛磺胆酸(TC),牛磺去氧胆酸(TCDC),牛磺去氧胆酸盐(TDC)及其混合物对人正常食管粘膜的影响方法:将人正常食管粘膜上皮细胞用无血清角质形成细胞培养基培养。 3- [4,5-二甲基噻唑基] -2,5-二苯基溴化四氮唑测定用于细胞增殖的检测。通过相差视频显微镜和末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)分析观察到了凋亡形态。 Sub-G1 DNA片段化和早期凋亡细胞通过碘化丙啶(PI)染色和膜联蛋白V-FITC与PI染色偶联的流式细胞仪(FCM)进行分析。结果:琼脂糖凝胶电泳观察到凋亡的DNA阶梯。结果:除GC外,GCDC,GDC,TC,TCDC,TDC及其混合物均可引起食管粘膜上皮细胞的生长抑制,呈剂量和时间依赖性。 TUNEL和FCM分析表明,除了GC外,500μmol/ L的胆汁​​盐和1500μmol/ L的混合物可诱导细胞凋亡。通过FCM进行PI染色检测到的sub-G1百分比在以500μmol/ L TC处理2小时的细胞中为83.5%,在以500μmol/ L TC处理的细胞中为19.8%,20.4%,25.6%,13.5%和75.8%。 / L GCDC,TCDC,GDC,TDC和1500μmol/ L混合物分别放置24 h,高于对照(1.5%)。在具有500μmol/ L GC的细胞中放置24小时的百分比为1.4%。在500μmol/ L TC处理2 h和1500μmol/ L混合物处理24 h后,在琼脂糖凝胶电泳上观察到DNA阶梯。诱导人正常食管粘膜上皮细胞凋亡,但GC对细胞的耐受性良好。

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