范冬梅,杨圆圆,姜琳琳.融合蛋白anti-CD19(Fab)-LDM对B细胞淋巴瘤BJAB细胞杀伤作用及其机制研究[J].中国肿瘤,2019,28(3):220-226.
融合蛋白anti-CD19(Fab)-LDM对B细胞淋巴瘤BJAB细胞杀伤作用及其机制研究
Cytotoxicity of Engineered Fusion Protein Anti-CD19(Fab)-LDM on B-cell Lymphoma BJAB Cells and Its Mechanism
投稿时间:2018-09-05  
DOI:10.11735/j.issn.1004-0242.2019.03.A011
中文关键词:  基因工程抗体  融合蛋白  力达霉素  B细胞淋巴瘤  细胞周期
英文关键词:genetic engineered antibody  fusion protein  lidamycin  B-cell lymphoma  cell cycle
基金项目:国家科技重大专项(2012ZX09102301)
作者单位
范冬梅 中国医学科学院北京协和医学院血液病医院血液学研究所 实验血液学国家重点实验室 
杨圆圆 中国医学科学院北京协和医学院血液病医院血液学研究所 实验血液学国家重点实验室 
姜琳琳 中国医学科学院北京协和医学院血液病医院血液学研究所 实验血液学国家重点实验室 
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中文摘要:
      摘 要:[目的] 探讨融合蛋白anti-CD19(Fab)-LDM对B细胞淋巴瘤细胞株BJAB细胞的杀伤作用及其机制研究。[方法] 利用流式细胞分析技术(FACS)和激光共聚焦显微镜技术,检测融合蛋白anti-CD19(Fab)-LDM与BJAB细胞的结合活性。MTT法检测融合蛋白anti-CD19(Fab)-LDM对BJAB细胞的体外杀伤活性。彗星电泳实验检测融合蛋白anti-CD19(Fab)-LDM对BJAB细胞DNA的损伤。FACS检测不同浓度融合蛋白anti-CD19(Fab)-LDM处理BJAB细胞后细胞周期的变化。 [结果] FACS和激光共聚焦显微镜技术实验结果表明,融合蛋白anti-CD19(Fab)-LDM能与BJAB细胞结合。MTT法实验结果表明,融合蛋白anti-CD19(Fab)-LDM对BJAB细胞杀伤活性较单用力达霉素或阿霉素强,IC50值分别为(0.15±0.02)nmol/L、(0.38±0.03)nmol/L 和(57.15±2.30)nmol/L。彗星电泳实验结果表明,用5pmol/L的融合蛋白anti-CD19(Fab)-LDM及力达霉素处理BJAB细胞后,可引起细胞不同程度的DNA损伤,由于融合蛋白anti-CD19(Fab)-LDM具有靶向性和细胞内化的特性,对DNA造成的损伤较力达霉素组明显。FACS结果显示,随着融合蛋白anti-CD19(Fab)-LDM浓度的增加,S期的比例从53.78%升高至77.29%,呈剂量依赖性。[结论] 融合蛋白anti-CD19(Fab)-LDM可以靶向杀伤B细胞淋巴瘤细胞株BJAB,引起细胞周期阻滞,在B细胞淋巴瘤生物治疗中具有潜在的应用价值。
英文摘要:
      Abstract:[Purpose] To investigate the cytotoxicity of the engineered fusion protein anti-CD19 (Fab)-LDM to B-cell lymphoma BJAB cells and its mechanism.[Methods] The antigen binding activity of anti-CD19(Fab)-LDM on BJAB cells was observed by FACS and confocal microscopy. The cytotoxicity of the engineered fusion protein anti-CD19(Fab)-LDM to BJAB cells was tested by MTT assay. Comet assay was used to determine the DNA damage in BJAB cells induced by anti-CD19(Fab)-LDM. Changes of cell cycle of BJAB cells treated with anti-CD19(Fab)-LDM were detected by FACS. [Results] FACS and confocal microscopy showed that the antibody bound specifically to BJAB cells. MTT assay demonstrated that the engineered fusion protein anti-CD19(Fab)-LDM strongly enhanced the cytotoxicity to BJAB cells compared with adriamycin or lidamycin (LDM). The comet assay showed that cells treated with anti-CD19(Fab)-LDM induced more DNA damage than cells treated with LDM. BJAB cells treated with anti-CD19(Fab)-LDM resulted in cell cycle arrest in a concentration dependence manner.[Conclusion] The fusion protein anti-CD19(Fab)-LDM can target to kill CD19-positive B lymphoma cells and induce cell cycle arrest. These findings may be useful in clinical practice for B-cell lymphoma treatment.
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