Glycogen synthase kinase-3 is essential for Treg development and function

T<sub>regs</sub> are critical regulators of the immune response, but the cellular and metabolic signaling pathways that control their development and homeostasis remain to be determined. We found that glycogen synthase kinase-3 (GSK3), a kinase that integrates signals from Akt and mTOR, was essential for T<sub>reg</sub> development, restraining fatal autoimmunity. Loss of Gsk3 led to metabolic rewiring in T<sub>regs</sub>, with disordered nucleotide metabolism and activation of OxPhos. Acute deletion of Gsk3 did not affect T<sub>reg</sub> frequency or numbers but induced an effector gene expression program and led to the formation of populations with pro-inflammatory signatures. The acute loss of Gsk3 in T<sub>regs</sub> profoundly enhanced anti-tumoral immune responses and suppressed tumor growth. Overall, we demonstrate that GSK3 critically regulates T<sub>reg</sub> homeostasis and anti-tumor immune responses.

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Publication Details

Journal
Cell Reports
Published
2025-09-01
DOI
https://doi.org/10.1016/j.celrep.2025.116256
Citations
1
Primary Topic
Genetics and Neurodevelopmental Disorders
Type
article
Field-Weighted Citation Impact
1.82
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article

Glycogen synthase kinase-3 is essential for Treg development and function

Matheswaran Kandasamy, Salvatore Valvo, Alexander J. Clarke, Moustafa Attar et al.
1 citations
Cell Reports
Genetics and Neurodevelopmental Disorders
1.82
article

Glycogen synthase kinase-3 is essential for Treg development and function

Matheswaran Kandasamy, Salvatore Valvo, Alexander J. Clarke, Moustafa Attar, Iwan G. A. Raza, Robert J. Mitchell, Barbara Kronsteiner, Mohammad A. Ali, Mariana Borsa, Hana F. Andrew
article en
1 citations

Abstract

T<sub>regs</sub> are critical regulators of the immune response, but the cellular and metabolic signaling pathways that control their development and homeostasis remain to be determined. We found that glycogen synthase kinase-3 (GSK3), a kinase that integrates signals from Akt and mTOR, was essential for T<sub>reg</sub> development, restraining fatal autoimmunity. Loss of Gsk3 led to metabolic rewiring in T<sub>regs</sub>, with disordered nucleotide metabolism and activation of OxPhos. Acute deletion of Gsk3 did not affect T<sub>reg</sub> frequency or numbers but induced an effector gene expression program and led to the formation of populations with pro-inflammatory signatures. The acute loss of Gsk3 in T<sub>regs</sub> profoundly enhanced anti-tumoral immune responses and suppressed tumor growth. Overall, we demonstrate that GSK3 critically regulates T<sub>reg</sub> homeostasis and anti-tumor immune responses.

Cell ReportsVol. 44(9)
Angkor Hospital for Children (KH), University of Oxford (GB), Kennedy Center (DK), Medawar Building for Pathogen Research (GB)
Openalex Percentile: Top 13%
Genetics and Neurodevelopmental Disorders
1.82
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Glycogen synthase kinase-3 is essential for Treg development and function — Matheswaran Kandasamy, Salvatore Valvo, et al. · Cell Reports (2025) | TGRS Research Map | TGRS