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题名

Reprogramming alternative macrophage polarization by GATM-mediated endogenous creatine synthesis: A potential target for HDM-induced asthma treatment

作者
通讯作者Li,Shun; Zhou,Xiaohui; Chen,Shanze; Chen,Rongchang
发表日期
2022-09-13
DOI
发表期刊
EISSN
1664-3224
卷号13
摘要
Cellular energy metabolism plays a crucial role in the regulation of macrophage polarization and in the execution of immune functions. A recent study showed that Slc6a8-mediated creatine uptake from exogenous supplementation modulates macrophage polarization, yet little is known about the role of the de novo creatine de novobiosynthesis pathway in macrophage polarization. Here, we observed that glycine amidinotransferase (GATM), the rate-limiting enzyme for creatine synthesis, was upregulated in alternative (M2) polarized macrophages, and was dependent on the transcriptional factor STAT6, whereas GATM expression was suppressed in the classical polarized (M1) macrophage. Next, we revealed that exogenous creatine supplementation enhanced IL-4-induced M2 polarization, confirming recent work. Furthermore, we revealed that genetic ablation of GATM did not affect expression of M1 marker genes (Nos2, IL1b, IL12b) or the production of nitric oxide in both peritoneal macrophages (PMs) and bone marrow-derived macrophages (BMDMs). By contrast, expression levels of M2 markers (Arg1, Mrc1, Ccl17 and Retnla) were lower following GATM deletion. Moreover, we found that deletion of GATM in resident alveolar macrophages (AMs) significantly blocked M2 polarization but with no obvious effect on the number of cells in knockout mice. Lastly, an upregulation of GATM was found in lung tissue and bronchoalveolar lavage fluid macrophages from HDM-induced asthmatic mice. Our study uncovers a previously uncharacterized role for the de novo creatine biosynthesis enzyme GATM in M2 macrophage polarization, which may be involved in the pathogenesis of related inflammatory diseases such as an T helper 2 (Th2)-associated allergic asthma.
关键词
相关链接[Scopus记录]
收录类别
语种
英语
学校署名
第一 ; 通讯
资助项目
Sichuan Province Science and Technology Support Program[2019YFS0230];Natural Science Foundation of Guangdong Province[2022A1515011966];National Natural Science Foundation of China[81803183];National Natural Science Foundation of China[82170042];Shenzhen Science and Technology Innovation Program[JCYJ20210324114400002];
WOS记录号
WOS:000861371300001
Scopus记录号
2-s2.0-85138985461
来源库
Scopus
引用统计
被引频次[WOS]:11
成果类型期刊论文
条目标识符http://sustech.caswiz.com/handle/2SGJ60CL/406205
专题南方科技大学医学院
南方科技大学第一附属医院
作者单位
1.Department of Pulmonary and Critical Care Medicine,The First Affiliated Hospital (Shenzhen People’s Hospital),School of Medicine,Southern University of Science and Technology,Shenzhen,China
2.Department of Animal Model,Shanghai Public Health Clinical Center,Fudan University,Shanghai,China
第一作者单位南方科技大学医学院;  南方科技大学第一附属医院
通讯作者单位南方科技大学医学院;  南方科技大学第一附属医院
第一作者的第一单位南方科技大学医学院;  南方科技大学第一附属医院
推荐引用方式
GB/T 7714
Yu,Li,Wang,Lingwei,Hu,Guang,et al. Reprogramming alternative macrophage polarization by GATM-mediated endogenous creatine synthesis: A potential target for HDM-induced asthma treatment[J]. Frontiers in Immunology,2022,13.
APA
Yu,Li.,Wang,Lingwei.,Hu,Guang.,Ren,Laibin.,Qiu,Chen.,...&Chen,Rongchang.(2022).Reprogramming alternative macrophage polarization by GATM-mediated endogenous creatine synthesis: A potential target for HDM-induced asthma treatment.Frontiers in Immunology,13.
MLA
Yu,Li,et al."Reprogramming alternative macrophage polarization by GATM-mediated endogenous creatine synthesis: A potential target for HDM-induced asthma treatment".Frontiers in Immunology 13(2022).
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