Cargando…

BACH2 restricts NK cell maturation and function, limiting immunity to cancer metastasis

Natural killer (NK) cells are critical to immune surveillance against infections and cancer. Their role in immune surveillance requires that NK cells are present within tissues in a quiescent state. Mechanisms by which NK cells remain quiescent in tissues are incompletely elucidated. The transcripti...

Descripción completa

Detalles Bibliográficos
Autores principales: Imianowski, Charlotte J., Whiteside, Sarah K., Lozano, Teresa, Evans, Alexander C., Benson, Jayme D., Courreges, Christina J.F., Sadiyah, Firas, Lau, Colleen M., Zandhuis, Nordin D., Grant, Francis M., Schuijs, Martijn J., Vardaka, Panagiota, Kuo, Paula, Soilleux, Elizabeth J., Yang, Jie, Sun, Joseph C., Kurosaki, Tomohiro, Okkenhaug, Klaus, Halim, Timotheus Y.F., Roychoudhuri, Rahul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9529614/
https://www.ncbi.nlm.nih.gov/pubmed/36178457
http://dx.doi.org/10.1084/jem.20211476
_version_ 1784801535729860608
author Imianowski, Charlotte J.
Whiteside, Sarah K.
Lozano, Teresa
Evans, Alexander C.
Benson, Jayme D.
Courreges, Christina J.F.
Sadiyah, Firas
Lau, Colleen M.
Zandhuis, Nordin D.
Grant, Francis M.
Schuijs, Martijn J.
Vardaka, Panagiota
Kuo, Paula
Soilleux, Elizabeth J.
Yang, Jie
Sun, Joseph C.
Kurosaki, Tomohiro
Okkenhaug, Klaus
Halim, Timotheus Y.F.
Roychoudhuri, Rahul
author_facet Imianowski, Charlotte J.
Whiteside, Sarah K.
Lozano, Teresa
Evans, Alexander C.
Benson, Jayme D.
Courreges, Christina J.F.
Sadiyah, Firas
Lau, Colleen M.
Zandhuis, Nordin D.
Grant, Francis M.
Schuijs, Martijn J.
Vardaka, Panagiota
Kuo, Paula
Soilleux, Elizabeth J.
Yang, Jie
Sun, Joseph C.
Kurosaki, Tomohiro
Okkenhaug, Klaus
Halim, Timotheus Y.F.
Roychoudhuri, Rahul
author_sort Imianowski, Charlotte J.
collection PubMed
description Natural killer (NK) cells are critical to immune surveillance against infections and cancer. Their role in immune surveillance requires that NK cells are present within tissues in a quiescent state. Mechanisms by which NK cells remain quiescent in tissues are incompletely elucidated. The transcriptional repressor BACH2 plays a critical role within the adaptive immune system, but its function within innate lymphocytes has been unclear. Here, we show that BACH2 acts as an intrinsic negative regulator of NK cell maturation and function. BACH2 is expressed within developing and mature NK cells and promotes the maintenance of immature NK cells by restricting their maturation in the presence of weak stimulatory signals. Loss of BACH2 within NK cells results in accumulation of activated NK cells with unrestrained cytotoxic function within tissues, which mediate augmented immune surveillance to pulmonary cancer metastasis. These findings establish a critical function of BACH2 as a global negative regulator of innate cytotoxic function and tumor immune surveillance by NK cells.
format Online
Article
Text
id pubmed-9529614
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-95296142023-03-30 BACH2 restricts NK cell maturation and function, limiting immunity to cancer metastasis Imianowski, Charlotte J. Whiteside, Sarah K. Lozano, Teresa Evans, Alexander C. Benson, Jayme D. Courreges, Christina J.F. Sadiyah, Firas Lau, Colleen M. Zandhuis, Nordin D. Grant, Francis M. Schuijs, Martijn J. Vardaka, Panagiota Kuo, Paula Soilleux, Elizabeth J. Yang, Jie Sun, Joseph C. Kurosaki, Tomohiro Okkenhaug, Klaus Halim, Timotheus Y.F. Roychoudhuri, Rahul J Exp Med Brief Definitive Report Natural killer (NK) cells are critical to immune surveillance against infections and cancer. Their role in immune surveillance requires that NK cells are present within tissues in a quiescent state. Mechanisms by which NK cells remain quiescent in tissues are incompletely elucidated. The transcriptional repressor BACH2 plays a critical role within the adaptive immune system, but its function within innate lymphocytes has been unclear. Here, we show that BACH2 acts as an intrinsic negative regulator of NK cell maturation and function. BACH2 is expressed within developing and mature NK cells and promotes the maintenance of immature NK cells by restricting their maturation in the presence of weak stimulatory signals. Loss of BACH2 within NK cells results in accumulation of activated NK cells with unrestrained cytotoxic function within tissues, which mediate augmented immune surveillance to pulmonary cancer metastasis. These findings establish a critical function of BACH2 as a global negative regulator of innate cytotoxic function and tumor immune surveillance by NK cells. Rockefeller University Press 2022-09-30 /pmc/articles/PMC9529614/ /pubmed/36178457 http://dx.doi.org/10.1084/jem.20211476 Text en © 2022 Imianowski et al. https://creativecommons.org/licenses/by-nc-sa/4.0/http://www.rupress.org/terms/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Brief Definitive Report
Imianowski, Charlotte J.
Whiteside, Sarah K.
Lozano, Teresa
Evans, Alexander C.
Benson, Jayme D.
Courreges, Christina J.F.
Sadiyah, Firas
Lau, Colleen M.
Zandhuis, Nordin D.
Grant, Francis M.
Schuijs, Martijn J.
Vardaka, Panagiota
Kuo, Paula
Soilleux, Elizabeth J.
Yang, Jie
Sun, Joseph C.
Kurosaki, Tomohiro
Okkenhaug, Klaus
Halim, Timotheus Y.F.
Roychoudhuri, Rahul
BACH2 restricts NK cell maturation and function, limiting immunity to cancer metastasis
title BACH2 restricts NK cell maturation and function, limiting immunity to cancer metastasis
title_full BACH2 restricts NK cell maturation and function, limiting immunity to cancer metastasis
title_fullStr BACH2 restricts NK cell maturation and function, limiting immunity to cancer metastasis
title_full_unstemmed BACH2 restricts NK cell maturation and function, limiting immunity to cancer metastasis
title_short BACH2 restricts NK cell maturation and function, limiting immunity to cancer metastasis
title_sort bach2 restricts nk cell maturation and function, limiting immunity to cancer metastasis
topic Brief Definitive Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9529614/
https://www.ncbi.nlm.nih.gov/pubmed/36178457
http://dx.doi.org/10.1084/jem.20211476
work_keys_str_mv AT imianowskicharlottej bach2restrictsnkcellmaturationandfunctionlimitingimmunitytocancermetastasis
AT whitesidesarahk bach2restrictsnkcellmaturationandfunctionlimitingimmunitytocancermetastasis
AT lozanoteresa bach2restrictsnkcellmaturationandfunctionlimitingimmunitytocancermetastasis
AT evansalexanderc bach2restrictsnkcellmaturationandfunctionlimitingimmunitytocancermetastasis
AT bensonjaymed bach2restrictsnkcellmaturationandfunctionlimitingimmunitytocancermetastasis
AT courregeschristinajf bach2restrictsnkcellmaturationandfunctionlimitingimmunitytocancermetastasis
AT sadiyahfiras bach2restrictsnkcellmaturationandfunctionlimitingimmunitytocancermetastasis
AT laucolleenm bach2restrictsnkcellmaturationandfunctionlimitingimmunitytocancermetastasis
AT zandhuisnordind bach2restrictsnkcellmaturationandfunctionlimitingimmunitytocancermetastasis
AT grantfrancism bach2restrictsnkcellmaturationandfunctionlimitingimmunitytocancermetastasis
AT schuijsmartijnj bach2restrictsnkcellmaturationandfunctionlimitingimmunitytocancermetastasis
AT vardakapanagiota bach2restrictsnkcellmaturationandfunctionlimitingimmunitytocancermetastasis
AT kuopaula bach2restrictsnkcellmaturationandfunctionlimitingimmunitytocancermetastasis
AT soilleuxelizabethj bach2restrictsnkcellmaturationandfunctionlimitingimmunitytocancermetastasis
AT yangjie bach2restrictsnkcellmaturationandfunctionlimitingimmunitytocancermetastasis
AT sunjosephc bach2restrictsnkcellmaturationandfunctionlimitingimmunitytocancermetastasis
AT kurosakitomohiro bach2restrictsnkcellmaturationandfunctionlimitingimmunitytocancermetastasis
AT okkenhaugklaus bach2restrictsnkcellmaturationandfunctionlimitingimmunitytocancermetastasis
AT halimtimotheusyf bach2restrictsnkcellmaturationandfunctionlimitingimmunitytocancermetastasis
AT roychoudhurirahul bach2restrictsnkcellmaturationandfunctionlimitingimmunitytocancermetastasis