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作 者:郑桂彬[1] 孟宪瑛[1] 韩佳滨 张强[1] 杨帅[1]
机构地区:[1]吉林大学第一医院甲状腺外科,长春130021
出 处:《中华内分泌外科杂志》2014年第5期398-401,共4页Chinese Journal of Endocrine Surgery
基 金:吉林省卫生厅科研课题(2008Z017)
摘 要:目的 观察在肿瘤坏死因子相关凋亡诱导配体(tumor necrosis factor-related apoptosis-inducing ligand,TRAIL)作用下甲状腺髓样癌TT细胞自噬发生情况,明确自噬在TRAIL诱导甲状腺癌TT细胞凋亡中的作用.方法 采用MTT法检测细胞增殖抑制率;MDC染色检测自噬的发生情况;流式细胞仪检测细胞凋亡;Western blot检测相关蛋白的表达.结果 ①MTT实验显示:TRAIL对TT细胞增殖抑制作用弱,在浓度为250、500、1000、2000 ng/ml的TRAIL作用48 h后对TT细胞增殖抑制率分别为(3.02±1.82)%、(4.87±1.45)%、(7.51±1.57)%及(12.76±3.23)%;②TRAIL作用48 h后,胞内代表自噬小体的绿色荧光亮点明显增多,且随TRAIL浓度的增加而增加;③3-MA预处理TT细胞4h,TRAIL 500 ng/ml及1000 ng/ml的凋亡率分别为(17.83 ±1.54)%及(27.81±1.79)%,明显高于单用TRAIL(3.70±0.34、6.55 ±0.59)%与3-MA (7.71±0.64)%之和,差异有统计学意义(t=3.282,P<0.05;t=7.830,P<0.01).④各实验组可见明显的caspase-8的活化裂解片段,自噬相关蛋白Beclin 1的表达明显减低.结论 甲状腺髓样癌TT细胞对TRAIL不敏感,TRAIL能诱导TT细胞内自噬发生,抑制自噬可明显改善TT细胞对TRAIL的敏感性.Objective To observe the level of autophagy induced by TRAIL in TT cell line and identify the role of autophagy in TRAIL-inducing apoptosis of TT cell line.Methods The growth inhibition of TT cells was measured by MTT assay.MDC staining was used to identify the happening of autophagy.Annexin V/PI double staining was used to analyze the apoptosis rate of TT cells by flowcytometry.The protein expression of caspase-8 and Beclin1 was detected by Western blot.Results ① The growth inhibition ratio of TT cells induced by TRAIL at the concentration of 250,500,1000 and 2000 ng/ml was (3.02 ± 1.82)%,(4.87 ± 1.45)%,(7.51 ± 1.57) %,(12.76 ± 3.23) % respectively,which suggested significant resistance of TT cells to TRAIL.② MDC-labeled green light vesicles was significantly increased after the treatment of TRAIL for 48 h.③ The apoptosis rate of TT cells induced by TRAIL at the concentration of 500 ng/ml and 1000 ng/ml after the pretreat ment of 3-MA for 4 h was(17.83 ± 1.54) % and(27.81 ± 1.79) % respectively,which was significantly higher than the apoptosis rate induced by TRAIL(3.70 ± 0.34) %,(6.55 ± 0.59) % alone and that induced by 3-MA(7.71 ± 0.64) % (t =3.282,P < 0.05 ; t =7.830,P < 0.01).④ The combination treatment of TRAIL and 3-MA increased the cleavage of caspase-8 and down-regulated the expression of Beclin 1.Conclusion Autophagy induced by TRAIL may contributes to the resistance of TT cells to TRAIL,which can be reversed by the inhibition of autophagy.
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