基础医学与临床 ›› 2015, Vol. 35 ›› Issue (8): 1055-1060.

• 研究论文 • 上一篇    下一篇

IL-2通过Jak3-Stat5通路促进巨噬细胞M1极化

亓文静,李岩,王玉,于爱莲   

  1. 泰山医学院
  • 收稿日期:2014-12-09 修回日期:2015-03-21 出版日期:2015-08-05 发布日期:2015-07-15
  • 通讯作者: 于爱莲 E-mail:alyu@tsmc.edu.cn
  • 基金资助:
    山东省科技发展计划项目

IL-2 promotes macrophage M1 polarization via the Jak3-Stat5 signaling pathway

  • Received:2014-12-09 Revised:2015-03-21 Online:2015-08-05 Published:2015-07-15

摘要: 目的 探究IL-2在调控巨噬细胞极化分型方面的作用及机制。方法 重组小鼠白介素-2 (IL-2)刺激处于M0期的小鼠单核巨噬细胞RAW 264.7,同时以IL-4作为对照。Real-time PCR和Western blot检测M1型和M2型标志分子的表达;流式细胞术检测M1型和M2型巨噬细胞的百分比;Western blot检测Jak3和Stat5活化水平。结果 经IL-2刺激后,处于M0的RAW 264.7细胞显著上调表达M1型标记分子,如IL-1β、IL-12、TNF-α和iNOS等;IL-2使巨噬细胞中M1型的比例由3.2%上升到24.6%,同时Jak3和Stat5分子的磷酸化水平显著提高。结论 IL-2具有促进巨噬细胞由M0向M1极化的作用,且该作用可能是通过Jak3-Stat5通路实现。

关键词: IL-2, IL-4, 巨噬细胞, 极化, Jak3-Stat5通路

Abstract: Objective To explore the effects and related mechanisms of Interleukin-2 (IL-2) on macrophage polarization. Methods Comparing with the recombinant mouse IL-4 (rmIL-4), rmIL-2 was used to treat the mouse macrophage cells RAW 264.7. Then, the cell markers of M1 and M2 expression were detected by Real-time PCR and Western blot. And the percentage of M1 or M2 macrophages was analyzed by flow cytometry. Additionally, the activation of Jak3 and Stat5 was also analyzed by Western blot. Results The expression of M1 maekers (IL-1β, IL-12, TNF-α and iNOS) was significantly up-regulated in RAW 264.7 cells after treated with IL-2. And the IL-2 treatment increased the percentage of M1 macrophages from 3.2% to 24.6%. Further, IL-2 significantly enhanced the phosphorylation of Jak3 and Stat5. Conclusions IL-2 could promote M1 polarization of macrophages, probably via the Jak3-Stat5 signaling pathway.

Key words: IL-2, IL-4, macrophage, polarization, Jak3-Stat5 signaling

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