题名 | Glutaredoxin 1 regulates macrophage polarization through mediating glutathionylation ofSTAT1 |
作者 | |
通讯作者 | Guo, Lijuan |
发表日期 | 2020-09-07
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DOI | |
发表期刊 | |
ISSN | 1759-7706
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EISSN | 1759-7714
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卷号 | 11期号:10页码:2966-2974 |
摘要 | Background Macrophage polarization affects tumor growth, metabolism, and many other tumor processes. M1 macrophages can promote antitumor immunity response. Signal transducer and activator of transcription 1 (STAT1) is one of the critical transcription factors in this process, which promotes the expression of a series of inflammatory molecules. STAT1 has been reported as a potential target of reactive oxygen species (ROS)-induced glutathionylation, while the glutathionylation of STAT1 in macrophages and its underlying regulatory mechanism remains unclear. Glutaredoxin 1 (Grx1) functions as a deglutathionylation enzyme, which regulates the activities of many proteins through reversing glutathionylation. Methods GeneChip and RT-qPCR was first applied to test the mRNA level of Grx1 in M1 macrophages. Western blot was then used to evaluate the variations of the Grx1 protein expression in M1 macrophages. Next, immunoprecipitation was used to investigate the glutathionylated STAT1 in both wild-type and Grx1(-/-)mouse macrophages. Finally, the induced alterations of STAT1 activity and function by Grx1 in M1 macrophage were examined by western blot and RT-qPCR. Results In M1-type macrophages, the levels of Grx1 were elevated. Glutathionylation of STAT1 was negatively regulated by Grx1. Furthermore, depletion of Grx1 increased the activity of STAT1, and thereby promoted the mRNA level of C-X-C motif chemokine ligand 9 (CXCL9) during M1-type polarization of macrophages. Conclusions Grx1 controlled deglutathionylation of STAT1, which in turn might regulate M1-type polarization of macrophages. |
关键词 | |
相关链接 | [来源记录] |
收录类别 | |
语种 | 英语
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学校署名 | 其他
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资助项目 | Sichuan Association for Science and Technology[2018RCTJ04]
; Innovation and Entrepreneurship Training Program for Sichuan University Students[C2019106935][C2020113908]
; National Natural Science Foundation of China[31401188][81470931]
; Science Foundation for Excellent Youth Scholars of Sichuan University Grant[2016SCU04A08]
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WOS研究方向 | Oncology
; Respiratory System
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WOS类目 | Oncology
; Respiratory System
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WOS记录号 | WOS:000566533700001
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出版者 | |
来源库 | Web of Science
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引用统计 |
被引频次[WOS]:9
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成果类型 | 期刊论文 |
条目标识符 | http://sustech.caswiz.com/handle/2SGJ60CL/186762 |
专题 | 南方科技大学第一附属医院 |
作者单位 | 1.Sichuan Univ, West China Sch Basic Med Sci & Forens Med, Dept Pathophysiol, Chengdu 610041, Peoples R China 2.Jinan Univ, Southern Univ Sci & Technol, Clin Med Coll 2,Key Lab Shenzhen Resp Dis, Affiliated Hosp,Shenzhen Peoples Hosp,Inst Resp D, Shenzhen, Peoples R China |
推荐引用方式 GB/T 7714 |
Guo, Lijuan,Chen, Shanze,Liu, Qingrong,et al. Glutaredoxin 1 regulates macrophage polarization through mediating glutathionylation ofSTAT1[J]. Thoracic Cancer,2020,11(10):2966-2974.
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APA |
Guo, Lijuan.,Chen, Shanze.,Liu, Qingrong.,Ren, Hongyu.,Li, Yuhao.,...&Li, Jingyu.(2020).Glutaredoxin 1 regulates macrophage polarization through mediating glutathionylation ofSTAT1.Thoracic Cancer,11(10),2966-2974.
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MLA |
Guo, Lijuan,et al."Glutaredoxin 1 regulates macrophage polarization through mediating glutathionylation ofSTAT1".Thoracic Cancer 11.10(2020):2966-2974.
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