USP28 protects development of inflammation in mouse intestine by regulating STAT5 phosphorylation and IL22 production in T lymphocytes.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2024
Historique:
received: 21 03 2024
accepted: 27 06 2024
medline: 30 7 2024
pubmed: 30 7 2024
entrez: 30 7 2024
Statut: epublish

Résumé

Ubiquitin-specific proteases (USPs), a large subset of more than 50 deubiquitinase proteins, have recently emerged as promising targets in cancer. However, their role in immune cell regulation, particularly in T cell activation, differentiation, and effector functions, remains largely unexplored. We utilized a USP28 knockout mouse line to study the effect of USP28 on T cell activation and function, and its role in intestinal inflammation using the dextran sulfate sodium (DSS)-induced colitis model and a series of in vitro assays. Our results show that USP28 exerts protective effects in acute intestinal inflammation. Mechanistically, USP28 knockout mice (USP28-/-) exhibited an increase in total T cells mainly due to an increased CD8+ T cell content. Additionally, USP28 deficiency resulted in early defects in T cell activation and functional changes. Specifically, we observed a reduced expression of IL17 and an increase in inducible regulatory T (iTreg) suppressive functions. Importantly, activated T cells lacking USP28 showed increased STAT5 phosphorylation. Consistent with these findings, these mice exhibited increased susceptibility to acute DSS-induced intestinal inflammation, accompanied by elevated IL22 cytokine levels. Our findings demonstrate that USP28 is essential for T cell functionality and protects mice from acute DSS-induced colitis by regulating STAT5 signaling and IL22 production. As a T cell regulator, USP28 plays a crucial role in immune responses and intestinal health.

Identifiants

pubmed: 39076972
doi: 10.3389/fimmu.2024.1401949
pmc: PMC11284026
doi:

Substances chimiques

STAT5 Transcription Factor 0
Interleukins 0
Interleukin-22 0
Ubiquitin Thiolesterase EC 3.4.19.12
Dextran Sulfate 9042-14-2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1401949

Informations de copyright

Copyright © 2024 Le Menn, Pikkarainen, Mennerich, Miroszewska, Kietzmann and Chen.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.

Auteurs

Gwenaëlle Le Menn (G)

Faculty of Biochemistry and Molecular Medicine, University of Oulu, Oulu, Finland.

Keela Pikkarainen (K)

Faculty of Biochemistry and Molecular Medicine, University of Oulu, Oulu, Finland.

Daniela Mennerich (D)

Faculty of Biochemistry and Molecular Medicine, University of Oulu, Oulu, Finland.

Dominika Miroszewska (D)

Intercollegiate Faculty of Biotechnology of University of Gdańsk and Medical University of Gdańsk, University of Gdańsk, Gdańsk, Poland.

Thomas Kietzmann (T)

Faculty of Biochemistry and Molecular Medicine, University of Oulu, Oulu, Finland.

Zhi Chen (Z)

Faculty of Biochemistry and Molecular Medicine, University of Oulu, Oulu, Finland.

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Classifications MeSH