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作 者:刘凌波[1] 黎纬明[1] 邹萍[1] 何伟[1] 张敏[1]
机构地区:[1]华中科技大学同济医学院附属协和医院血液病研究所,武汉430022
出 处:《中国实验血液学杂志》2006年第5期862-866,共5页Journal of Experimental Hematology
基 金:was supported by agrant from National Natural Sciences Foundation of China(No.30240022).
摘 要:为了研究抗Fas锤头状核酶对T细胞Fas表达及其凋亡的影响和探讨增强供者淋巴细胞输注时移植物抗白血病(GVL)效应的新策略,构建可有效切割FasmRNA的锤头状核酶真核质粒,用电穿孔法将其导入小鼠CTL细胞株CTLL-2之后,借助RT-PCR和Westernblot检测其Fas的表达,同时检测转染前后其胱冬酶-3(Caspase-3)活性和凋亡(AnnexinV-FITC法)的改变,并用MTT法检测空白对照组、空载体转染组及pU6-RZ596转染组CTLL-2细胞的增殖情况和体外杀伤小鼠急性粒-单核白血病细胞(WEHI-3)的活性。结果表明:构建的U6嵌合型锤头状核酶RZ596在细胞内能有效切割Fas,明显降低小鼠活化CTLL-2的Fas水平,与高表达Fas配体的WEHI-3孵育后,其存活率和体外杀伤WEHI-3活性明显高于对照组。结论:抗Fas核酶能显著降低小鼠活化CTLL-2的Fas表达,使其免于WEHI-3的膜Fas配体经Fas途径所致的凋亡,并提高CTL对小鼠急性粒-单核白血病细胞的杀伤力,从而阻抑小鼠急性粒-单核白血病细胞的免疫逃逸。In order to investigate the inhibition role of anti-Fas hammerhead ribozyme on Fas expression and Fas-mediated apoptosis in CTLL-2 ceils( mouse CTL cell line), and to explore a new way for enhancing the ability of T cells against Leukemia in donor lymphoeytes infusion, CTLL-2 cells were transfected with pEGFP-RZ596 and pEGFPCI (mock-transfeeted) via eleetroporation. Fas expression on CTLL-2 cells was detected by RT-PCR and Western blot. The killing effect of CTL against WEHI-3 ( mouse acute myelomonoeytic leukemia cell line) highly expressing FasL in vitro was detected by MTT assay. The caspase-3 proteolyfic activity and the apoptosis rate of CTLL-2 ceils were detected by means of BD AproAlert Caspase-3 Colorimetric kit and FITC labeled Annexin-V apoptosis detecting kit respectively. The results showed that the anti-Fas ribozyme could be successfully introduced into mouse CTLL-2 cells; Fas expression on the surface of ceils transfected with the ribozyme was obviously decreased, in comparison with control and mocktransfected ceils; after cocultured with WEHI-3 cells, the viability of CTLL-2 ceils transfeced with the ribozyme was significantly increased , as compared with other two groups; caspase-3 activity and apoptosis rate of the ribozyme-transfeced ceils were significantly decreased, the killing effect of CTLL-2 transfected with the ribozyme was stronger than that of other groups. It is concluded that anti-Fas ribozyme can remarkably decrease Fas expression on CTLL-2 ceils, so as to avoid Fas-mediated apoptosis by Fas ligand on WEHI-3 cells, and to enhance their killing activity against WEHI-3 ceils, as a result, the immune escape of acute myelomonocytic leukemia was depressed.
关 键 词:Fas核酶 细胞毒T淋巴细胞(CTL) 急性粒-单核细胞白血病 免疫逃逸
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