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Natural killer cells limit the clearance of senescent lung adenocarcinoma cells

Senescence is an important p53-controlled tumor suppressor program that not only opposes the proliferation of cancer cells but also promotes their immune-mediated clearance in certain contexts. In hepatocellular cancer, p53 induction promotes an innate immune cell-mediated clearance of senescent cel...

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Autores principales: Stokes, Kate L., Cortez-Retamozo, Virna, Acosta, Jonuelle, Lauderback, Brian, Robles-Oteiza, Camila, Cicchini, Michelle, Pittet, Mikael J., Feldser, David M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443683/
https://www.ncbi.nlm.nih.gov/pubmed/30936429
http://dx.doi.org/10.1038/s41389-019-0133-3
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author Stokes, Kate L.
Cortez-Retamozo, Virna
Acosta, Jonuelle
Lauderback, Brian
Robles-Oteiza, Camila
Cicchini, Michelle
Pittet, Mikael J.
Feldser, David M.
author_facet Stokes, Kate L.
Cortez-Retamozo, Virna
Acosta, Jonuelle
Lauderback, Brian
Robles-Oteiza, Camila
Cicchini, Michelle
Pittet, Mikael J.
Feldser, David M.
author_sort Stokes, Kate L.
collection PubMed
description Senescence is an important p53-controlled tumor suppressor program that not only opposes the proliferation of cancer cells but also promotes their immune-mediated clearance in certain contexts. In hepatocellular cancer, p53 induction promotes an innate immune cell-mediated clearance of senescent cells wherein natural killer (NK) cells seem to play the primary sentinel role. Whether NK cells also surveil cancer cells in other tumor types when p53 is activated to promote a senescence response is unknown. To identify the role that NK and other innate immune cell types have on the surveillance and destruction of lung adenocarcinoma cells, we developed an orthotopic transplantation model where p53 gene function could be restored to induce senescence after successful engraftment of tumor cells in the mouse lung. Contrary to precedent, we found that NK cells actually limited the efficient clearance of tumor cells from the mouse lung after p53 restoration. Instead, activation of p53 induced the infiltration of monocytes, neutrophils, and interstitial macrophages. Loss of NK cells further promoted expansion of these inflammatory cell types and tumor clearance after p53 restoration. These observations suggest that NK cell responses to p53 activation in lung adenocarcinoma is distinct from those found in other tumor types and that diverse innate immune cell populations may play context-dependent roles during tumor immune surveillance. Further, our data provide an impetus to understand the broader mechanisms that regulate cancer cell destruction by multiple cell types of the innate immune system and distinct cancer contexts.
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spelling pubmed-64436832019-04-02 Natural killer cells limit the clearance of senescent lung adenocarcinoma cells Stokes, Kate L. Cortez-Retamozo, Virna Acosta, Jonuelle Lauderback, Brian Robles-Oteiza, Camila Cicchini, Michelle Pittet, Mikael J. Feldser, David M. Oncogenesis Article Senescence is an important p53-controlled tumor suppressor program that not only opposes the proliferation of cancer cells but also promotes their immune-mediated clearance in certain contexts. In hepatocellular cancer, p53 induction promotes an innate immune cell-mediated clearance of senescent cells wherein natural killer (NK) cells seem to play the primary sentinel role. Whether NK cells also surveil cancer cells in other tumor types when p53 is activated to promote a senescence response is unknown. To identify the role that NK and other innate immune cell types have on the surveillance and destruction of lung adenocarcinoma cells, we developed an orthotopic transplantation model where p53 gene function could be restored to induce senescence after successful engraftment of tumor cells in the mouse lung. Contrary to precedent, we found that NK cells actually limited the efficient clearance of tumor cells from the mouse lung after p53 restoration. Instead, activation of p53 induced the infiltration of monocytes, neutrophils, and interstitial macrophages. Loss of NK cells further promoted expansion of these inflammatory cell types and tumor clearance after p53 restoration. These observations suggest that NK cell responses to p53 activation in lung adenocarcinoma is distinct from those found in other tumor types and that diverse innate immune cell populations may play context-dependent roles during tumor immune surveillance. Further, our data provide an impetus to understand the broader mechanisms that regulate cancer cell destruction by multiple cell types of the innate immune system and distinct cancer contexts. Nature Publishing Group UK 2019-04-01 /pmc/articles/PMC6443683/ /pubmed/30936429 http://dx.doi.org/10.1038/s41389-019-0133-3 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Stokes, Kate L.
Cortez-Retamozo, Virna
Acosta, Jonuelle
Lauderback, Brian
Robles-Oteiza, Camila
Cicchini, Michelle
Pittet, Mikael J.
Feldser, David M.
Natural killer cells limit the clearance of senescent lung adenocarcinoma cells
title Natural killer cells limit the clearance of senescent lung adenocarcinoma cells
title_full Natural killer cells limit the clearance of senescent lung adenocarcinoma cells
title_fullStr Natural killer cells limit the clearance of senescent lung adenocarcinoma cells
title_full_unstemmed Natural killer cells limit the clearance of senescent lung adenocarcinoma cells
title_short Natural killer cells limit the clearance of senescent lung adenocarcinoma cells
title_sort natural killer cells limit the clearance of senescent lung adenocarcinoma cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443683/
https://www.ncbi.nlm.nih.gov/pubmed/30936429
http://dx.doi.org/10.1038/s41389-019-0133-3
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