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A spatial map of human macrophage niches reveals context-dependent macrophage functions in colon and breast cancer

Tumor-associated macrophages (TAMs) display heterogeneous phenotypes. Yet the exact tissue cues that shape macrophage functional diversity are incompletely understood. Here we discriminate, spatially resolve and reveal the function of five distinct macrophage niches within malignant and benign breas...

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Autores principales: Matusiak, Magdalena, Hickey, John W., Luca, Bogdan, Lu, Guolan, Kidziński, Lukasz, Zhu, Shirley, Colburg, Deana Rae Crystal, Phillips, Darci J., Brubaker, Sky W., Charville, Gregory W., Shen, Jeanne, Nolan, Garry P., Newman, Aaron M., West, Robert B., van de Rijn, Matt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9882614/
https://www.ncbi.nlm.nih.gov/pubmed/36711732
http://dx.doi.org/10.21203/rs.3.rs-2393443/v1
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author Matusiak, Magdalena
Hickey, John W.
Luca, Bogdan
Lu, Guolan
Kidziński, Lukasz
Zhu, Shirley
Colburg, Deana Rae Crystal
Phillips, Darci J.
Brubaker, Sky W.
Charville, Gregory W.
Shen, Jeanne
Nolan, Garry P.
Newman, Aaron M.
West, Robert B.
van de Rijn, Matt
author_facet Matusiak, Magdalena
Hickey, John W.
Luca, Bogdan
Lu, Guolan
Kidziński, Lukasz
Zhu, Shirley
Colburg, Deana Rae Crystal
Phillips, Darci J.
Brubaker, Sky W.
Charville, Gregory W.
Shen, Jeanne
Nolan, Garry P.
Newman, Aaron M.
West, Robert B.
van de Rijn, Matt
author_sort Matusiak, Magdalena
collection PubMed
description Tumor-associated macrophages (TAMs) display heterogeneous phenotypes. Yet the exact tissue cues that shape macrophage functional diversity are incompletely understood. Here we discriminate, spatially resolve and reveal the function of five distinct macrophage niches within malignant and benign breast and colon tissue. We found that SPP1 TAMs reside in hypoxic and necrotic tumor regions, and a novel subset of FOLR2 tissue resident macrophages (TRMs) supports the plasma cell tissue niche. We discover that IL4I1 macrophages populate niches with high cell turnover where they phagocytose dying cells. Significantly, IL4I1 TAMs abundance correlates with anti-PD1 treatment response in breast cancer. Furthermore, NLRP3 inflammasome activation in NLRP3 TAMs correlates with neutrophil infiltration in the tumors and is associated with poor outcome in breast cancer patients. This suggests the NLRP3 inflammasome as a novel cancer immunetherapy target. Our work uncovers context-dependent roles of macrophage subsets, and suggests novel predictive markers and macrophage subset-specific therapy targets.
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spelling pubmed-98826142023-01-28 A spatial map of human macrophage niches reveals context-dependent macrophage functions in colon and breast cancer Matusiak, Magdalena Hickey, John W. Luca, Bogdan Lu, Guolan Kidziński, Lukasz Zhu, Shirley Colburg, Deana Rae Crystal Phillips, Darci J. Brubaker, Sky W. Charville, Gregory W. Shen, Jeanne Nolan, Garry P. Newman, Aaron M. West, Robert B. van de Rijn, Matt Res Sq Article Tumor-associated macrophages (TAMs) display heterogeneous phenotypes. Yet the exact tissue cues that shape macrophage functional diversity are incompletely understood. Here we discriminate, spatially resolve and reveal the function of five distinct macrophage niches within malignant and benign breast and colon tissue. We found that SPP1 TAMs reside in hypoxic and necrotic tumor regions, and a novel subset of FOLR2 tissue resident macrophages (TRMs) supports the plasma cell tissue niche. We discover that IL4I1 macrophages populate niches with high cell turnover where they phagocytose dying cells. Significantly, IL4I1 TAMs abundance correlates with anti-PD1 treatment response in breast cancer. Furthermore, NLRP3 inflammasome activation in NLRP3 TAMs correlates with neutrophil infiltration in the tumors and is associated with poor outcome in breast cancer patients. This suggests the NLRP3 inflammasome as a novel cancer immunetherapy target. Our work uncovers context-dependent roles of macrophage subsets, and suggests novel predictive markers and macrophage subset-specific therapy targets. American Journal Experts 2023-01-10 /pmc/articles/PMC9882614/ /pubmed/36711732 http://dx.doi.org/10.21203/rs.3.rs-2393443/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Matusiak, Magdalena
Hickey, John W.
Luca, Bogdan
Lu, Guolan
Kidziński, Lukasz
Zhu, Shirley
Colburg, Deana Rae Crystal
Phillips, Darci J.
Brubaker, Sky W.
Charville, Gregory W.
Shen, Jeanne
Nolan, Garry P.
Newman, Aaron M.
West, Robert B.
van de Rijn, Matt
A spatial map of human macrophage niches reveals context-dependent macrophage functions in colon and breast cancer
title A spatial map of human macrophage niches reveals context-dependent macrophage functions in colon and breast cancer
title_full A spatial map of human macrophage niches reveals context-dependent macrophage functions in colon and breast cancer
title_fullStr A spatial map of human macrophage niches reveals context-dependent macrophage functions in colon and breast cancer
title_full_unstemmed A spatial map of human macrophage niches reveals context-dependent macrophage functions in colon and breast cancer
title_short A spatial map of human macrophage niches reveals context-dependent macrophage functions in colon and breast cancer
title_sort spatial map of human macrophage niches reveals context-dependent macrophage functions in colon and breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9882614/
https://www.ncbi.nlm.nih.gov/pubmed/36711732
http://dx.doi.org/10.21203/rs.3.rs-2393443/v1
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