基础医学与临床 ›› 2012, Vol. 32 ›› Issue (5): 505-509.

• 研究论文 • 上一篇    下一篇

约氏疟MIF对小鼠BM-DC细胞作用的探索

王恒,罗茗月,邵丁丁   

  1. 中国医学科学院基础医学研究所 北京协和医学院基础学院
  • 收稿日期:2012-01-13 修回日期:2012-03-21 出版日期:2012-05-05 发布日期:2012-04-16
  • 通讯作者: 王恒 E-mail:wanghpumc@126.com
  • 基金资助:
    国家重点基础研究发展计划

Influence of P.yoelii MIF on mouse BM-DC

  • Received:2012-01-13 Revised:2012-03-21 Online:2012-05-05 Published:2012-04-16

摘要: 摘要:目的 探索约氏疟原虫来源巨噬细胞迁移抑制因子(PyMIF)对小鼠髓系树突状细胞(BM-DC)表型和功能的影响。方法分离小鼠骨髓细胞并经GM-CSF和IL-4诱导培养得到BM-DC:经PyMIF刺激后,通过流式细胞术检测其TLR2、TLR4、CD80、CD86、CD40、MHCII分子表达,通过ELISA方法检测IL-12、IL-10分泌;经PyMIF刺激的BM-DC与CD4+T或CD8+T细胞共培养,同样方法检测T细胞CD69表达、IL-2分泌情况,并检测CD8+T细胞对靶细胞杀伤能力。结果PyMIF可以下调小鼠骨髓来源树突状细胞TLR-4的表达;但不能影响BM-DC细胞表面分子TLR2、CD80、CD86、CD40、MHCII的表达,也不改变BM-DC分泌IL-12、IL-10。PyMIF可通过BM-DC下调CD8+T的CD69表达,但不能通过BM-DC改变CD4+T细胞CD69表达、IL-2分泌,及CD8+T细胞IL-2分泌。结论PyMIF可能是通过下调BM-DC细胞TLR4表达来抑制免疫细胞对疟原虫的识别,使之逃逸机体的攻击而存活。

关键词: 疟原虫来源巨噬细胞迁移抑制因子, 骨髓来源巨噬细胞, TLR4, CD69

Abstract: Abstract: Objective Detect the role of P.yoelii plasmodium derived macrophage migration inhibitory factor (PyMIF) recombination protein on the phenotype and function of bone marrow dendritic cells (BM-DC). Methods : BM-DC induced from bone marrow precursors were treated with PyMIF or MmMIF,then cell surface molecular such as TLR2、TLR4、CD80、CD86、CD40、MHCII were detected by flow cytometry and IL-12、IL-10 were analyzed by ELISA. PyMIF or MmMIF treated BM-DC were first stimulated by LPS,then co-cultured with CD4+T or CD8+T cells, CD69 and IL-2 were detected as previously described to indentify the activity of T cells. What’s more, the tytotoxic action of CD8+T was also measured. Results: PyMIF decreased the TLR4 expression of BM-DC,but had neither effect on TLR2、CD80、CD86、CD40 and MHCII expression, nor influence on IL12、IL-10 secreting. What is more, PyMIF down-regulated CD69 expression of CD8+T through BM-DC, and could not influence CD69 expression and IL-2 secrecting of CD4+T and IL-2 secrecting of CD8+T cells through BM-DC. Conclusion:PyMIF could down-regulated TLR4 expression of BM-DC to prevent being attacked by immune system, so as to survive in the organism.

Key words: PyMIF, BM-DC , TLR4, CD69