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作 者:李玉华[1] 郭坤元[1] 陈慧[2] 李江琪[1] 王丰[3] 谢匡诚[3] 韦毅[2] 黄建生[2] 任大明[2]
机构地区:[1]第一军医大学附属珠江医院血液科,广州510282 [2]复旦大学遗传研究所国家重点实验室 [3]上海市第一人民医院
出 处:《中华血液学杂志》2001年第5期235-237,共3页Chinese Journal of Hematology
基 金:国家自然科学基金!资助项目 (3 9870 3 3 0 )
摘 要:目的 观察Ly49A基因转染的C5 7BL/ 6小鼠的淋巴细胞对BALB/c小鼠正常成纤维细胞和 4T1乳腺癌细胞杀伤能力的变化与差异。方法 构建逆转录病毒表达载体pLXSN Ly49A ,经由PA317包装细胞包装后转染C5 7BL/ 6小鼠淋巴细胞。流式细胞仪检测Ly49A受体在转染后淋巴细胞上的表达率。MTT法检测转染后淋巴细胞对BALB/c小鼠正常成纤维细胞和 4T1乳腺癌细胞的杀伤活性 ,以空载体转染和未转染的淋巴细胞作对照。结果 Ly49A基因转染的C5 7BL/ 6小鼠的淋巴细胞 2 4h后Ly49A受体表达率为 (4 6 .6 7± 0 .35 ) % ,空载体转染组为 (18.73± 0 .85 ) % ,未转染对照组为 (19.6 0± 0 .2 7) % ,其对BALB/c小鼠正常成纤维细胞的杀伤活性明显降低 (抑制率 2 2 %~ 2 5 % ) ,对 4T1乳腺癌细胞的杀伤活性无明显改变 (P >0 .0 5 )。结论 转染Ly49A的C5 7BL/ 6小鼠淋巴细胞对BALB/c小鼠正常细胞的杀伤作用明显降低 ,但仍保留了对肿瘤细胞的杀伤活性 。Objective To observe the killing activities of Ly49A gene transfected lymphocytes of C57BL/6 mice to normal and tumor cells of BALB/c mice. Methods pLXSN Ly49A retrovirus vector was constructed and packaged with PA317 cell line. The lymphocytes of C57BL/6 mice were transfected by culture with virus producing PA317 cells. The Ly49A expression rate on the transfected lymphocytes was detected by flow cytometry and the killing activities of the transfected lymphocytes to normal and tumor cells of BALB/c mice were assayed by MTT method. Results The Ly49A expression rates of C57BL/6 mice lymphocytes transfected with pLXSN Ly49A for 24 hours, of those transfected with pLXSN and nontransfected control were (46.67±0.35)%,(18.73±0 85)%,and (19.60±0.27)%, respectively. The killing activity of the transfected lymphocytes to 4T 1 tumor cells remained almost the same as that of the control (P>0.05), but to normal fibroblasts decreased sharply (inhibiting rate 22%~25%). Conclusion The Ly49A transfected C57BL/6 mice lymphocytes could kill BALB/c mice tumor cells as effectively as the control did, but the activity decreased sharply to normal BALB/c mice cells, which would be instructive for resolving graft versus host disease after allogeneic bone marrow transplantation.
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