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小鼠肝癌细胞(H22)源外泌体的体内抗肝癌作用研究

Antitumor effects of exosomes derived from a mouse hepatoma carcinoma cell line H22

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【作者】 李静沈宜杨麟段红郑维平

【Author】 LI Jing,SHEN Yi,YANG Lin,DUAN Hong,ZHENG Wei-ping (Department of Pathophysiology,College of Basic Medicine,Chongqing Medical University,Chongqing 400016,China)

【机构】 重庆医科大学基础医学院病理生理教研室

【摘要】 目的在荷瘤动物模型观察小鼠肝癌细胞(H22)来源的外泌体(exosomes)激发宿主抗肝癌免疫应答的效应。方法用自行分离纯化的小鼠肝癌细胞H22源外泌体免疫小鼠,然后给小鼠皮下注射H22肿瘤细胞,观察肿瘤的生长状况。用MTT法检测小鼠脾细胞增殖情况和细胞毒活性;用免疫组织化学法检测肿瘤组织中CD4+、CD8+T淋巴细胞浸润情况。结果该外泌体使肿瘤出现时间延迟,肿瘤生长缓慢,小鼠生存率提高。促进脾淋巴细胞增殖并增强其细胞毒活性,促进CD4+和CD8+T细胞活化。结论小鼠肝癌细胞(H22)源外泌体能诱导抗肿瘤应答,有效地诱导特异性的杀伤肿瘤细胞活性,有针对亲本细胞的免疫保护作用。

【Abstract】 Objective To investigate the induction of antitumor response and its immune mechanism of H22 cell-derived exosomes. Methods Fifteen BALB/c mice were immunized by H22 cell-derived exosomes three times at weekly intervals,then inoculated with the wild-type H22. Another 15 BALB/c mice that were injected with PBS were used as controls. In the 80-day observation period,the tumor growth and survival time were observed. MTT was used to determine lymphocyte proliferation and specific cytotoxicity of mice splenic cells. Immunohistochemical staining of CD4+ and CD8+ was performed for lymphocyte infiltration in tumor tissues. Results Immunization with exosomes derived from H22 delayed the tumor growth and promoted the survival rate of the mice bearing the tumor,and also induced lymphocyte proliferation and triggered strong specific cytotoxic response of spleen lymphocytes and activated CD4+ and CD8+ T cells. Conclusion Vaccination of H22 cell-derived exosomes is effective in inducing the protective immunity. Furthermore,those exosomes have strong antitumor activities.

  • 【文献出处】 第三军医大学学报 ,Acta Academiae Medicinae Militaris Tertiae , 编辑部邮箱 ,2008年19期
  • 【分类号】R735.7
  • 【被引频次】4
  • 【下载频次】569
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