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同种大鼠骨髓间充质干细胞诱导调节性B淋巴细胞的免疫负调节作用 被引量:5

An experimental study on the role of MSCs in inducing regulatory B cells and the underlying mechanisms
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摘要 目的研究骨髓间充质干细胞(MSC)诱导调节性B淋巴细胞(Breg细胞)的免疫负调节作用。方法取DA大鼠MSC和Lewis大鼠B淋巴细胞共培养后,酶联免疫吸附试验(EUSA)检测MSC和B淋巴细胞混合培养组上清液中白细胞介素10(IL-10)的水平和分泌因子的变化;采用流式细胞技术分析B淋巴细胞增殖、凋亡、表型的变化和对抗原特异性T淋巴细胞增殖的影响,采用激光共聚焦显微镜观察Breg细胞对免疫复合物吞噬能力的变化。结果MS(2成功诱导产生高分泌IL-10的Breg细胞产生,表型为CDl9+CDld+CD5+,MSC显著抑制B淋巴细胞的增殖,Breg细胞能抑制抗原特异性T淋巴细胞的增殖,并增加对免疫复合物的吞噬能力。结论MS(2诱导的Breg细胞具有明显的免疫负调节作用。 Objective To observe the immunoregulatory roles of MSCs in inducing proliferation of B regulatory cells (Bregs). Method DA Rat MSCs were co-cultured with Wistar rat B ceils. The levels of IL-10 and secrete proinflammatory cytokines in the supematants were determined by using ELISA. The proliferation and apoptosis of B cells after interaction with MSCs were analyzed by using FACS. In order to investigate whether Bregs are involved in the phagocytosis of immune complex (IC), B ceils and Bregs were incubated with FITC-OVA IC. The fluorescence intensity was detected by using immunofluorescence microscopy. Results MSCs induced B cells to differentiate into Bregs with high CD19, CDld and CD5 expression and high IL-10 level. The proliferation of B cells was significantly suppressed after interaction with MSCs. Bregs had enhanced phagocytic capacity as compared with that of B cells. Bregs significantly inhibited maDC-induced CD4+ T cell proliferation compared to B cells, without depressing IL-2 or IFN-7 secretion. Conclusion MSCs induce freshly isolated B cells to differentiate into Bregs characterized by the ability to preferentially produce IL-10.
作者 王月 牛坚
出处 《中华器官移植杂志》 CAS CSCD 北大核心 2013年第7期428-431,共4页 Chinese Journal of Organ Transplantation
基金 国家自然科学基金项目资助,江苏省333人才项目
关键词 大鼠 间质干细胞 B淋巴细胞 免疫耐受 Rats Mesenchymal stem cells B-Lymphocytes Immune tolerance
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参考文献9

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同被引文献42

  • 1Qian-Qian Chen,Li Yan,Chang-Zheng Wang,Wei-Hua Wang,Hui Shi,Bin-Bin Su,Qing-Huan Zeng,Hai-Tao Du,Jun Wan.Mesenchymal stem cells alleviate TNBS-induced colitis by modulating inflammatory and autoimmune responses[J].World Journal of Gastroenterology,2013,19(29):4702-4717. 被引量:25
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