南方医科大学学报 ›› 2013, Vol. 33 ›› Issue (01): 121-.

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脐带源间充质干细胞可增强自然杀伤细胞对树突状细胞的杀伤活性

赵一俏,曹东林,陈伟   

  • 出版日期:2013-01-20 发布日期:2013-01-20

Regulation of mesenchymal stem cells derived from umbilical cord on natural killer cells-mediated cytotoxicity against dendritic cells

  • Online:2013-01-20 Published:2013-01-20

摘要: 目的观察脐带源间充质干细胞对自然杀伤细胞杀伤树突状细胞的影响,初步探讨其作用机制。方法胶原酶消化整个
脐带组织,体外培养间充质干细胞;分离健康人外周血单个核细胞,磁珠分选树突状细胞。在白介素-4和粒单-集落刺激因子共
同作用下获得大量未成熟树突状细胞,将脐带源间充质干细胞与未成熟树突状细胞共培养2 d,同时加入肿瘤坏死因子α,诱导
树突状细胞成熟。流式细胞术检测诱导后树突状细胞CD11c和CD86的表达,ELISA法检测培养液中白介素-12的含量,乳酸
脱氢酶释放法检测自然杀伤细胞对树突状细胞的杀伤活性,流式细胞术检测树突状细胞表面自然杀伤细胞活化性受体的配体
(MICA/B和ULBP1-3)的表达。结果与单纯细胞因子诱导比较,脐带源间充质干细胞诱导后树突状细胞CD11c的表达无明显
差异,但CD86的表达降低,IL-12的分泌量降低。自然杀伤细胞对脐带源间充质干细胞诱导后的树突状细胞的杀伤效率明显高
于单纯细胞因子诱导后的树突状细胞。与单纯细胞因子诱导比较,脐带源间充质干细胞诱导后的树突状细胞活化性受体的配
体(MICA和MICB)的表达增高。结论脐带源间充质干细胞能增强自然杀伤细胞对树突状细胞的杀伤活性,这可能与脐带源
间充质干细胞抑制树突状细胞成熟,上调树突状细胞表面自然杀伤细胞活化性受体的配体有关。

Abstract: Objective To observe the effect of mesenchymal stem cells derived from umbilical cord (UC-MSCs) on natural killer
(NK) cells-mediated cytotoxicity against dendritic cells (DCs) and explore the mechanism. Methods MSCs were isolated from
human umbilical cord by collagen digestion and cultured in vitro. NK cells were separated from healthy human peripheral
blood by magnetic bead sorting. Mononuclear cells from healthy human peripheral blood were cultured in the presence of
granulocyte and macrophage colony stimulating factor (GM-CSF) and interleukin-4 (IL-4) to obtain the immature DCs. The
DCs were then co-cultured with UC-MSCs in the presence of tumor necrosis factor α (TNFα) for 2 days, and the expressions of
CD11c and CD86 on DCs and IL-12 level in the culture medium was detected using flow cytometry and ELISA, respectively.
The cytotoxicity of NK cells against DCs was analyzed by LDH-releasing assay, and the expressions of ligands for killer
activator receptor (MICA/B and ULBP1-3) on the DCs were detected with flow cytometry. Results Compared with the
cytokine-induced DCs, the DCs induced by co-culture with UC-MSCs showed an identical CD11c expression but lowered
CD86 expression and IL-12 secretion. The natural killer cells produced a stronger cytotoxicity against UC-MSCs-induced DCs
than against cytokine-induced DCs. The UC-MSCs-induced DCs also showed increased expressions of MICA and MICB on the
surface. Conclusion UC-MSCs can enhance NK cells-mediated cytotoxicity against DCs possibly by inhibiting DC maturation
and up-regulating the ligands for killer activator receptor on the surface of the DCs.