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作 者:张颖妹[1] 徐秀珍[1] 刘红涛[1] 宋泉声[1] 马大龙[1]
机构地区:[1]北京医科大学卫生部医学免疫学重点实验室,北京100083
出 处:《中国免疫学杂志》2000年第1期8-11,共4页Chinese Journal of Immunology
基 金:国家自然科学基金!39870427
摘 要:目的:对一种新发现的凋亡相关基因TFAR19进行蛋白质水平的促凋亡效应研究,并对其作用机理进行初步的探讨。方法;利用离子交换层析对大肠杆菌表达的人重组TFAR19蛋白进行纯化,将其加入到培养的白血病细胞株HL-60,通过DNA片段化、PI及AnnekinV标记进行流式细胞仪分析,观察TFAR19蛋白的促凋亡效应。利用FITC标记TFAR19蛋白,分析其与细胞的结合及定位。利用Caspase-3抑制剂DEVD-fmk研究TFAR19的凋亡信号转导途径。结果:高纯度的重组TFAR19蛋白剂量依赖性地促进撤除血清的HL-60细胞的凋亡,最高可使82%细胞凋亡,对照为30%。荧光标记的TFAN19蛋白能与HL-60细胞结合,主要定位于细胞核。DEVK-fmk可部分抑制TFAR19蛋白的促凋亡效应。结论:TFAR19蛋白能够直接进入HL-60细胞,发挥其促进细胞凋亡的效应。这一效应部分地与Caspase-3的凋亡执行效应有关。Objective: To study the apoptosis-accelerating effect of a novel human protein named TFAR19 (TF-1 cells apoptosis relatedprotein 19) whose encoding cDNA has been cloned in the laboratory, and try to find out the mechanism of its effect. Methods: By using ionexchange chromatography , the human recombinant TFAR19 protein was isolated. The parified protein was occulted with HL-60 cells and theapoptotic cells were analyzed by DNA fragmentation, PI and Annexin V-labeled FACS assay. The FTTC labeled TFAR19 protein was used asprobe to observe its localization within the HL-60 cells. For the signal transduction study, a caspase-3 inhibitor DEVD-fmk was used to blockthe TFAR19 effect. Results: The TFAR19 Protein dose-dependently increases the apoptotic HL-60 cells which have been previously serum from culture, up to 82% cells are apoptotic cells comparing with control 30% cells. FITC labeled TFAR19 protein binds with HL-60Cells and mainly locallied within the nucleus. DEVD-fmk pahly inhibits apoptosis-accelerating effect of the TFAR19 protein. Conclusion:TFAR19 protein can directly enter HL-60 cells and exhibits an apoptosis-accelerating effect. Caspase-3 as an apoptosis effector may involve theeffect of TFAR19.
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