Divergent Role for STAT5 in the Adaptive Responses of Natural Killer Cells.


Journal

Cell reports
ISSN: 2211-1247
Titre abrégé: Cell Rep
Pays: United States
ID NLM: 101573691

Informations de publication

Date de publication:
15 12 2020
Historique:
received: 06 01 2020
revised: 09 10 2020
accepted: 17 11 2020
entrez: 16 12 2020
pubmed: 17 12 2020
medline: 22 12 2021
Statut: ppublish

Résumé

Natural killer (NK) cells are innate lymphocytes with the capacity to elicit adaptive features, including clonal expansion and immunological memory. Because signal transducer and activator of transcription 5 (STAT5) is essential for NK cell development, the roles of this transcription factor and its upstream cytokines interleukin-2 (IL-2) and IL-15 during infection have not been carefully investigated. In this study, we investigate how STAT5 regulates transcription during viral infection. We demonstrate that STAT5 is induced in NK cells by IL-12 and STAT4 early after infection and that partial STAT5 deficiency results in a defective capacity of NK cells to generate long-lived memory cells. Furthermore, we find a functional dichotomy of IL-2 and IL-15 signaling outputs during viral infection, whereby both cytokines drive clonal expansion, but only IL-15 is required for memory NK cell survival. We thus highlight a role for STAT5 signaling in promoting an optimal anti-viral NK cell response.

Identifiants

pubmed: 33326784
pii: S2211-1247(20)31487-X
doi: 10.1016/j.celrep.2020.108498
pmc: PMC7773031
mid: NIHMS1657047
pii:
doi:

Substances chimiques

STAT5 Transcription Factor 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

108498

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI100874
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI130043
Pays : United States

Informations de copyright

Copyright © 2020 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Interests The authors declare no competing interests.

Auteurs

Gabriela M Wiedemann (GM)

Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; Department of Internal Medicine II, Technical University of Munich, Munich, Germany.

Simon Grassmann (S)

Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

Colleen M Lau (CM)

Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

Moritz Rapp (M)

Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

Alejandro V Villarino (AV)

Molecular Immunology and Inflammation Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, USA.

Christin Friedrich (C)

Würzburg Institute of Systems Immunology, Julius-Maximilians-Universität, 97078 Würzburg, Germany.

Georg Gasteiger (G)

Würzburg Institute of Systems Immunology, Julius-Maximilians-Universität, 97078 Würzburg, Germany.

John J O'Shea (JJ)

Molecular Immunology and Inflammation Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, USA.

Joseph C Sun (JC)

Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; Department of Immunology and Microbial Pathogenesis, Weill Cornell Medical College, New York, NY 10065, USA. Electronic address: sunj@mskcc.org.

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