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小鼠树突状细胞体外培养的实验研究

Experimental study of mice DCs culture in vitro
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摘要 目的研究体外大量扩增小鼠树突状细胞(DCs)的实验方法。方法用细胞因子[肿瘤坏死因子-α(TNF-α)、白介素-4(IL-4)、粒细胞-巨噬细胞集落刺激因子(GM-CSF)]组合体外诱导培养DCs,混合淋巴细胞实验检测DCs的免疫刺激活性。结果培养6-8 d,细胞表面有大量毛刺状突起生长,即DCs;该DCs具有很强的刺激T淋巴细胞增殖的能力,且在T细胞与DCs比值为10∶1时最强。结论 TNF-α、IL-4、GM-CSF组合是诱导体外扩增DCs的较佳方法。 Objective To study the experiment method for largely expanding mice dendritic cells(DCs) in vitro.Methods The lymphokines combined with tumor necrosis factor-α(TNF-α),interleukin-4(IL-4) and granulocyte-macrophage colonystimulating factor(GM-CSF) were adopted for inducing and cultivating DCs in vitro;the immunostimulatory activity of DCs was detected by the mixed lymphocyte reaction.Results The cell surface exhibited a large number of burr-lke process on 6-8 d of culture,i.e.,DCs;the cultured DCs had the ability to strongly immunostimulate the proliferation of T lymphocytes,which with the T cells/DCs ratio of 10:1 was strongest.Conclusion The combination of TNF-α,IL-4 and GM-CSF is a better method for largely expanding mice DCs in vitro.
作者 蒋俊艳 曾波
出处 《现代医药卫生》 2013年第13期1972-1973,共2页 Journal of Modern Medicine & Health
关键词 树突细胞 肿瘤坏死因子α 白细胞介素4 粒细胞巨噬细胞集落刺激因子 淋巴因子 体外培养 小鼠 近交BALBC Dendritic cells Tumor necrosis factor-alpha Interleukin-4 Granulocyte-macrophage colony-stimulating factor Lymphokines Cultivation in vitro Mice inbred BALB C
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