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机构地区:[1]第三军医大学第一附属医院肿瘤科,重庆400038 [2]温州医科大学附属第一医院皮肤性病科,325000 [3]第三军医大学基础部免疫学教研室,重庆400038
出 处:《免疫学杂志》2013年第11期921-926,共6页Immunological Journal
基 金:国家自然科学基金面上项目(81071706)
摘 要:目的探讨黑色素瘤小鼠体内CD8+T淋巴细胞亚群的比例变化并对CD8+CD62L+CD127+T细胞亚群的功能做初步研究。方法将B16细胞注入C57/BL小鼠右腋皮下,制备黑色素瘤小鼠模型,4周后处死,用流式细胞术检测脾脏、血液及骨髓细胞中各CD8+T淋巴细胞亚群的比例变化,将升高的CD8+CD62L+CD127+T细胞群与肿瘤细胞共培养,流式检测其凋亡、ELISA检测共培养上清中IFN-γ的分泌水平;将CD8+CD62L+CD127+T细胞体外刺激后用MTT法检测其增殖情况。结果在B16荷瘤小鼠脾脏CD8+CD62L+、CD8+CD127+和CD8+CD62L+CD127+T细胞频率显著高于正常对照小鼠,外周血和骨髓中这些细胞的频率在2组小鼠之间无显著性差异。荷瘤小鼠体内CD8+CD62L+CD127+T细胞亚群IFN-γ分泌的能力低于CD8+CD62L+CD127-T细胞(P<0.05),也明显低于CD8+T细胞(P<0.01)。但相对于CD8+T细胞,CD8+CD62L+CD127+T增殖能力明显增强(P<0.01)而凋亡减弱(P<0.05)。结论 B16荷瘤小鼠脾脏中记忆CD8+T细胞亚群频率升高,而CD8+CD62L+CD127+T细胞亚群有更强的增殖能力和抗凋亡能力,提示小鼠黑色素瘤促进了记忆CD8+T细胞生成且CD8+CD62L+CD127+T细胞可能具有更独特的作用。To determine the variation of different CD8+ T cell subsets and the functions of the CD8+CD62L+ CD127+T cell subset in melanoma mice, BI6 cell was injected subcutaneously in right axilla of C57/BL mice to prepare a mouse model of melanoma. Four weeks after, flow cytometry was employed to detect the variation of different CD8+T cell subsets in spleen, blood and marrow cells of the model mice; and then using flow cytometry to detect the apoptosis and ELISA to detect the IFN-γ secretion after co-cultured CD8+CD62L+CD127+T cells with tumor cells. Furthermore, MTT assay was used to detect the proliferation of CD8+CD62L+CD127+T cells after in vitro stimulation. Results showed that the frequency of CD8+T cell subsets CD8+CD62L+, CDS+CD127+ and CD8+CD62L+CD127+T cell was significant higher than that of normal control mice. But the frequency of these cells in blood and bone marrow was no significant difference between the tumor-bearing mice and normal mice. The CD8+CD62L+CD127+T cell subsets in melanoma have lower capacity to secrete IFN-γ as compared with CD8+CD62L+CD127+T cells (P〈0.05) and CD8+ T cells (P〈 0.01). Furthermore, for C D 8+C D62L+CD127+T cell subset, their proliferation was significantly increased (P〈 0.01) and apoptosis was significantly diminished (P〈 0.05), compared with CD8+T cells. In conclusion, the percentage of memory CD8+T cell subsets is increased in B16 tumor-bearing mice, while CD8+CD62L+CD127+ cell subsets have a stronger ability of anti-apoptotie and proliferative capacity, suggesting that tumor-bearing mice promotes memory CD8+T cells generation and CD8+CD62L+CD127+ memory T cells may play more unique roles.
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