Gpx4 Regulates Invariant NKT Cell Homeostasis and Function by Preventing Lipid Peroxidation and Ferroptosis.


Journal

Journal of immunology (Baltimore, Md. : 1950)
ISSN: 1550-6606
Titre abrégé: J Immunol
Pays: United States
ID NLM: 2985117R

Informations de publication

Date de publication:
19 Aug 2024
Historique:
received: 06 05 2024
accepted: 29 07 2024
medline: 19 8 2024
pubmed: 19 8 2024
entrez: 19 8 2024
Statut: aheadofprint

Résumé

Invariant NKT (iNKT) cells are a group of innate-like T cells that plays important roles in immune homeostasis and activation. We found that iNKT cells, compared with CD4+ T cells, have significantly higher levels of lipid peroxidation in both mice and humans. Proteomic analysis also demonstrated that iNKT cells express higher levels of phospholipid hydroperoxidase glutathione peroxidase 4 (Gpx4), a major antioxidant enzyme that reduces lipid peroxidation and prevents ferroptosis. T cell-specific deletion of Gpx4 reduces iNKT cell population, most prominently the IFN-γ-producing NKT1 subset. RNA-sequencing analysis revealed that IFN-γ signaling, cell cycle regulation, and mitochondrial function are perturbed by Gpx4 deletion in iNKT cells. Consistently, we detected impaired cytokine production, elevated cell proliferation and cell death, and accumulation of lipid peroxides and mitochondrial reactive oxygen species in Gpx4 knockout iNKT cells. Ferroptosis inhibitors, iron chelators, vitamin E, and vitamin K2 can prevent ferroptosis induced by Gpx4 deficiency in iNKT cells and ameliorate the impaired function of iNKT cells due to Gpx4 inhibition. Last, vitamin E rescues iNKT cell population in Gpx4 knockout mice. Altogether, our findings reveal the critical role of Gpx4 in regulating iNKT cell homeostasis and function, through controlling lipid peroxidation and ferroptosis.

Identifiants

pubmed: 39158281
pii: 267089
doi: 10.4049/jimmunol.2400246
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : HHS | NIH | National Institute of General Medical Sciences (NIGMS)
ID : GM-147713
Organisme : HHS | NIH | National Institute of General Medical Sciences (NIGMS)
ID : GM-147713-02S1
Organisme : HHS | NIH | National Institute of General Medical Sciences (NIGMS)
ID : GM-139763
Organisme : Presbyterian Health Foundation (PHF)
ID : Collaborative Research Grant
Organisme : HHS | NIH | National Institute of General Medical Sciences (NIGMS)
ID : GM-137786
Organisme : HHS | NIH | National Institute of General Medical Sciences (NIGMS)
ID : GM-103447
Organisme : HHS | NIH | NIH Office of the Director (OD)
ID : S10OD028479
Organisme : HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI)
ID : HL-145454

Informations de copyright

Copyright © 2024 by The American Association of Immunologists, Inc.

Auteurs

Sophia P M Sok (SPM)

Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK.

Kaitlyn Pipkin (K)

Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK.

Narcis I Popescu (NI)

Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK.

Megan Reidy (M)

Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK.

Bin Li (B)

Department of Cellular and Molecular Medicine, School of Medicine, University of California-San Diego, La Jolla, CA.

Holly Van Remmen (H)

Aging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK.
Oklahoma City Veterans Affairs Medical Center, Oklahoma City, OK.

Mike Kinter (M)

Aging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK.

Xiao-Hong Sun (XH)

Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK.

Zhichao Fan (Z)

Department of Immunology, School of Medicine, UConn Health, Farmington, CT.

Meng Zhao (M)

Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK.
Department of Microbiology and Immunology, University of Oklahoma Health Science Center, Oklahoma City, OK.

Classifications MeSH