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机构地区:[1]武汉大学基础医学院病理生理学系,湖北武汉430071
出 处:《武汉大学学报(医学版)》2015年第3期354-358,共5页Medical Journal of Wuhan University
基 金:国家自然科学基金资助项目(编号:81270411)
摘 要:目的:探讨骨髓间充质干细胞(MSC)对单核细胞分化为树突状细胞(DC)的影响。方法:将分离培养的MSC与单核细胞共培养,加入DC分化诱导因子GM-CSF和IL-4(MSC+-DC),并以培养分化体系中无MSC存在的作为阳性对照(MSC--DC)。6d后收集悬浮细胞并用TNF-α诱导成熟48h。分别用流式细胞术、混合淋巴细胞反应及扫描电子显微镜检测细胞的表型、免疫功能及细胞形态。结果:同阳性对照DC相比,与MSC共培养得到的细胞上DC相关分子的表达明显较低,包括CD80,CD86,CD1a,CD83;而CD14分子则持续性高表达;与MSC共培养的细胞刺激异基因T淋巴细胞增殖的能力亦显著降低。形态学上,细胞胞体小,胞质突起不明显甚至缺如。结论:MSC抑制单核细胞向DC分化和成熟。Objective:To study the effects of bone marrow mesenchymal stem cells(MSCs)on the differentiation of DCs derived from monocytes.Methods:Monocytes were cultured with human MSCs in the presence of GM-CSF and IL-4.On day 6,cells in suspension were collected and TNF-αwas added to induce maturation of DCs for 48 hours.Phenotype,allogeneic stimulatory capacity and morphology of obtained cells were analyzed through cytometry,mixed lymphocyte reaction and scanning electronic microscopy.Results:Phenotypically,these cells expressed much lower levels of DC-related molecules,such as CD1 a,CD86,CD80 and CD83,whereas they expressed persistently high level of CD14.Functionally,their capacity to stimulate allogeneic T cells was significantly inhibited.Accordingly,these cells expressed rarely long and large cytoplasmic dendrites.Conclusion:MSCs inhibit the differentiation of monocytes into DCs.
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