PGC-1α通过线粒体介导巨噬细胞极化状态的机制研究

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PGC-1α通过线粒体介导巨噬细胞极化状态的机制研究

基础医学 | 更新时间：2026-01-09

- PGC-1α通过线粒体介导巨噬细胞极化状态的机制研究
- Mechanism of mitochondria-mediated PGC-1α in macrophage polarization
- 第三军医大学学报 2019年41卷第1期页码：56-62
- 作者机构：
  
  400010 重庆, 重庆医科大学附属第二医院乳甲外科
- 作者简介：
  
  [ 明佳，E-mail：mjia1001@sina.com MING Jia, E-mail: mjia1001@sina.com
- 基金信息：
  
  重庆市卫生计生委医学科研计划项目(2016ZDXM012);重庆技术创新与应用示范(社会民生类)一般项目(CSTC2018jscx-msybx0020);重庆市渝中区科技计划项目(20160104)
- DOI：10.16016/j.1000-5404.201808139
  中图分类号： R392.12;R73-362;R737.9
- 收稿：2018-08-20，
  
  修回：2018-11-07，
  
  纸质出版：2019-01-15
- 稿件说明：
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靳鑫, 倪田根, 王宁, 等. PGC-1α通过线粒体介导巨噬细胞极化状态的机制研究[J]. 第三军医大学学报, 2019,41(1):56-62.

Xin JIN, Tiangen NI, Ning WANG, et al. Mechanism of mitochondria-mediated PGC-1α in macrophage polarization[J]. Journal of Third Military Medical University, 2019, 41(1): 56-62.
靳鑫, 倪田根, 王宁, 等. PGC-1α通过线粒体介导巨噬细胞极化状态的机制研究[J]. 第三军医大学学报, 2019,41(1):56-62. DOI： 10.16016/j.1000-5404.201808139.

Xin JIN, Tiangen NI, Ning WANG, et al. Mechanism of mitochondria-mediated PGC-1α in macrophage polarization[J]. Journal of Third Military Medical University, 2019, 41(1): 56-62. DOI： 10.16016/j.1000-5404.201808139.

摘要

目的

2

探讨通过敲低PGC-1α对肿瘤相关巨噬细胞(tumor associated macrophages

TAMs)极化状态的影响及其机制。

方法

2

以小鼠腹腔巨噬细胞(mouse peritoneal macrophages，PMs)为研究对象，与4T1细胞共培养24 h建立TAMs；shRNA转染构建瞬时低表达PGC-1α的TAMs；Western blot检测TAMs中PGC-1α、TAMs极化指标、TAMs线粒体功能蛋白的蛋白表达；Real-time PCR(qRT-PCR)检测TAMs的mtDNA水平；流式细胞术检测TAMs极化标志物，ROS水平的变化；ATP测定试剂盒检测TAMs中ATP水平的变化。

结果

2

与PMs组比较，TAMs组PGC-1α蛋白表达上调(

P

<

0.05)，M2型分泌细胞因子蛋白(TGF-β1、IL-10)表达升高(

P

<

0.05)，线粒体功能相关蛋白(NRF-1、TFAM)表达升高(

P

<

0.05)，M2型极化标记物(CD206)表达升高(

P

<

0.05)，M1型分泌细胞因子蛋白(TNF-α、IL-1β)表达降低(

P

<

0.05)；sh-PGC-1α TAMs组较TAMs组发生了相反的变化，即PGC-1α蛋白表达降低(

P

<

0.05)，M2型分泌细胞因子蛋白(TGF-β1、IL-10)表达降低(

P

<

0.05)，线粒体功能相关

蛋白(NRF-1、TFAM)表达降低(

P

<

0.05)，M2型极化标记物(CD206)表达降低(

P

<

0.05)，M1型分泌细胞因子蛋白(TNF-α、IL-1β)表达升高(

P

<

0.05)，M1型极化标记物(CD86)表达升高(

P

<

0.05)。

结论

2

PGC-1α参与了乳腺TAMs向M2极化的过程，其机制可能为癌细胞与TAMs相互作用，增强了TAMs中依赖PGC-1α的线粒体功能，促使细胞向M2分化，并产生M2型细胞因子。

Abstract

Objective

2

To investigate the effect of knocking down peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) on the polarization in tumor-associated macrophages (TAMs).

Methods

2

Mouse peritoneal macrophages (PMs) were co-cultured with mouse mammary tumor cell line 4T1 for 24 h to establish TAMs. shRNAs sequence of PGC-1α was synthesized and transfected to construct TAMs with transient low expression of PGC-1α. Western blotting was used to detect the expression of PGC-1α and mitochondrial function-related proteins. Real-time PCR (qRT-PCR) was employed to measure the mtDNA levels

flow cytometry to detect macrophage polarization markers

reactive oxygen species (ROS) kit to test the generation of ROS

and ATP assay kit to study the ATP level in the TAMs.

Results

2

Compared with PMs

PGC-1α was up-regulated in TAMs (

P

<

0.05)

so were the M2-type secreted cytokines (TGF-β1 and IL-10) (

P

<

0.05)

mitochondrial function-related proteins [nuclear respiratory factor 1 (NRF1) and mitochondrial transcription factor A (TFAM)

]

(

P

<

0.05)

and M2 type polarization marker (CD206) (

P

<

0.05)

but the levels of M1 type secreted cytokines (TNF-α and IL-1β) were decreased (

P

<

0.05). sh-PGC-1α transfection led to opposite changes when compared with TAMs (all

P

<

0.05).

Conclusion

2

PGC-1α is involved in the polarization of breast TAMs to M2. The mechanism may be due to the interaction between the tumor cells and TAMs

which enhances the PGC-1α-dependent mitochondrial function in TAMs

promotes cell differentiation to M2

and then produces M2 cytokines.

关键词

Keywords

references

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