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山东大学学报(医学版) ›› 2016, Vol. 54 ›› Issue (10): 16-20.doi: 10.6040/j.issn.1671-7554.0.2015.1029

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脐带间充质干细胞对小胶质细胞增殖及活化的影响

王娜,陈乃耀   

  1. 华北理工大学附属医院血液内科, 河北 唐山 063000
  • 收稿日期:2015-10-29 出版日期:2016-10-10 发布日期:2016-10-10
  • 通讯作者: 陈乃耀. E-mail:nychenncmc@163.com E-mail:nychenncmc@163.com
  • 基金资助:
    河北省自然科学基金(H2013209253)

Effect of umbilical cord mesenchymal stem cells on microglial polarization and proliferation

WANG Na, CHEN Naiyao   

  1. Department of Hematology, Affiliated Hospital of North China University of Science and Technology, Tangshan 063000, Hebei, China
  • Received:2015-10-29 Online:2016-10-10 Published:2016-10-10

摘要: 目的 观察人脐带来源的间充质干细胞(hUC-MSCs)在正常环境和炎症环境下对小胶质细胞活化的调节作用,探讨hUC-MSCs对中枢神经系统炎症反应的免疫调节作用。 方法 将BV2细胞与人脐带间充质干细胞来源的条件培养基(hUC-MSCs-CM)和(或)脂多糖(LPS)共培养24或48 h后利用MTT比色法分析BV2增殖活力的变化,ELISA试剂盒分析BV2细胞上清中TNF-α和IL-6的变化,免疫印迹法检测精氨酸酶1(Arg1)的表达, Real-time PCR分析TNF-α、IL-6、ARG1基因的表达水平。 结果 (1)BV2在LPS长程刺激下表现出明显的增殖效应,而hUC-MSCs-CM可以抑制这种增殖反应;(2)炎症刺激诱导BV2表达TNF-α和IL-6明显增多,而在hUC-MSCs-CM和LPS共刺激时TNF-α和IL-6表达明显低于LPS单刺激组;(3)hUC-MSCs-CM共培养组BV2细胞高表达M2型小胶质细胞标志物Arg1。 结论 脐带间充质干细胞抑制炎症所致的小胶质细胞增殖;脐带间充质干细胞通过旁分泌机制调节小胶质细胞向M2型活化,降低促炎因子表达,这可能是其最终发挥神经保护作用的机制之一。

关键词: 神经保护作用, 脐带间充质干细胞, 免疫调节, 小胶质细胞

Abstract: Objective To observe the effect of umbilical cord mesenchymal stem cells(hUC-MSCs)on the microglia proliferation and activation in normal or inflammatory conditions, in order to explore their immunomodulation effect on the central nervous system. Methods After BV2 cells were co-cultured with hUC-MSCs-CM and/or lipopolysaccharide(LPS)for 24 or 48 h, the proliferation was analyzed by MTT colorimetric method, TNF-α and IL-6 in the supernatant were measured by ELISA kit, Arginase 1(Arg1)protein and mRNA levels were examined by Western blotting, TNF-α and IL-6 mRNA expression level were tested by real-time PCR. Results (1) After long-time LPS stimulation, BV2 cells obviously proliferated, while hUC-MSCs-CM inhibited the proliferation. (2) BV2 cultured with LPS expressed high levels of TNF-α and IL-6, while in both hUC-MSCs-CM and LPS conditions, the TNF-α and IL-6 levels were lower than in LPS stimulation. (3) The level of Arg1 was increased in BV2 cells co-cultured with hUC-MSCs-CM for 48 h. Conclusions Human UC-MSCs inhibit microglia proliferation caused by inflammatory stimulation. Human UC-MSCs induce microglial cells to M2 polarization and reduce the expression of proinflammatory factors via paracrine mechanism, and this may be the mechanism for its neuroprotective effect.

Key words: Neuroprotection, Immunomodulation, Microglia, Umbilical cord mesenchymal stem cells

中图分类号: 

  • R392.1
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