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E3泛素连接酶STUB1通过p62影响mTORC1信号通路,并参与类风湿关节炎中滤泡辅助性T细胞分化的调控。

E3 ubiquitin ligase STUB1 affects the mTORC1 pathway through p62 and participates in regulating the differentiation of follicular helper T cells in rheumatoid arthritis.

作者信息

Wang Wen, Yang Yachen, Shi Yujia, Xiang Ting, Xie Jianmin

机构信息

Department of Rheumatology, the Second Affiliated Hospital of Nanjing Medical University, Nanjing, China.

Department of Rheumatology, the Second Affiliated Hospital of Nanjing Medical University, Nanjing, China.

出版信息

Clin Immunol. 2023 Oct;255:109736. doi: 10.1016/j.clim.2023.109736. Epub 2023 Aug 20.

DOI:10.1016/j.clim.2023.109736
PMID:37604355
Abstract

OBJECTIVE

The abnormal expansion of Tfh cells plays a key role in chronic inflammation of RA joint. We speculated that STUB1 is an important regulatory factor in promoting the differentiation of Tfh cells in RA.

CONTENT AND METHODS

The proportion of Tfh cells and the level of STUB1 in Tfh cells was measured. CD4T cells were isolated from PBMCs of RA patients, and the percentage of Tfh cells was detected after up- or down-regulating the expression of STUB1. The levels of mTORC1 pathway activator p-mTOR and p-S6K were measured by Western blot. The ubiquitination of p62 by STUB1 and its ubiquitination type as well as the activation of mTORC1 was detected in vitro, and the activation of the mTORC1 and the differentiation of Tfh cells was detected in STUB1-upregulated CD4 T cells with overexpressed p62.

RESULTS

The level of STUB1 is elevated in Tfh cells of patients. Up-regulation of STUB1 can promote the differentiation of Tfh cells. STUB1 promotes the degradation of p62 via K48-linked ubiquitination and promotes the activation of mTORC1. Overexpression of p62 can reverse the promoting effect of STUB1 on the differentiation of Tfh cells and the activation of mTORC1.

CONCLUSION

STUB1 can promote the differentiation of Tfh cells in RA by mediating the activation of mTORC1 pathway through ubiquitination of p62.

摘要

目的

Tfh细胞异常扩增在类风湿关节炎(RA)关节慢性炎症中起关键作用。我们推测STUB1是促进RA中Tfh细胞分化的重要调节因子。

内容与方法

检测Tfh细胞的比例及Tfh细胞中STUB1的水平。从RA患者外周血单个核细胞(PBMCs)中分离CD4T细胞,上调或下调STUB1表达后检测Tfh细胞百分比。通过蛋白质免疫印迹法检测mTORC1途径激活剂p-mTOR和p-S6K的水平。在体外检测STUB1对p62的泛素化及其泛素化类型以及mTORC1的激活情况,并在过表达p62的STUB1上调的CD4 T细胞中检测mTORC1的激活和Tfh细胞的分化。

结果

患者Tfh细胞中STUB1水平升高。上调STUB1可促进Tfh细胞分化。STUB1通过K48连接的泛素化促进p62降解并促进mTORC1激活。过表达p62可逆转STUB1对Tfh细胞分化和mTORC1激活的促进作用。

结论

STUB1可通过p62泛素化介导mTORC1途径激活,促进RA中Tfh细胞分化。

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