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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...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Journal Experts
2023
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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. |
format | Online Article Text |
id | pubmed-9882614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Journal Experts |
record_format | MEDLINE/PubMed |
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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