Cargando…

Macrophages orchestrate the expansion of a proangiogenic perivascular niche during cancer progression

Tumor-associated macrophages (TAMs) are a highly plastic stromal cell type that support cancer progression. Using single-cell RNA sequencing of TAMs from a spontaneous murine model of mammary adenocarcinoma (MMTV-PyMT), we characterize a subset of these cells expressing lymphatic vessel endothelial...

Descripción completa

Detalles Bibliográficos
Autores principales: Opzoomer, James W., Anstee, Joanne E., Dean, Isaac, Hill, Emily J., Bouybayoune, Ihssane, Caron, Jonathan, Muliaditan, Tamara, Gordon, Peter, Sosnowska, Dominika, Nuamah, Rosamond, Pinder, Sarah E., Ng, Tony, Dazzi, Francesco, Kordasti, Shahram, Withers, David R., Lawrence, Toby, Arnold, James N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8565907/
https://www.ncbi.nlm.nih.gov/pubmed/34730997
http://dx.doi.org/10.1126/sciadv.abg9518
_version_ 1784593906337316864
author Opzoomer, James W.
Anstee, Joanne E.
Dean, Isaac
Hill, Emily J.
Bouybayoune, Ihssane
Caron, Jonathan
Muliaditan, Tamara
Gordon, Peter
Sosnowska, Dominika
Nuamah, Rosamond
Pinder, Sarah E.
Ng, Tony
Dazzi, Francesco
Kordasti, Shahram
Withers, David R.
Lawrence, Toby
Arnold, James N.
author_facet Opzoomer, James W.
Anstee, Joanne E.
Dean, Isaac
Hill, Emily J.
Bouybayoune, Ihssane
Caron, Jonathan
Muliaditan, Tamara
Gordon, Peter
Sosnowska, Dominika
Nuamah, Rosamond
Pinder, Sarah E.
Ng, Tony
Dazzi, Francesco
Kordasti, Shahram
Withers, David R.
Lawrence, Toby
Arnold, James N.
author_sort Opzoomer, James W.
collection PubMed
description Tumor-associated macrophages (TAMs) are a highly plastic stromal cell type that support cancer progression. Using single-cell RNA sequencing of TAMs from a spontaneous murine model of mammary adenocarcinoma (MMTV-PyMT), we characterize a subset of these cells expressing lymphatic vessel endothelial hyaluronic acid receptor 1 (Lyve-1) that spatially reside proximal to blood vasculature. We demonstrate that Lyve-1(+) TAMs support tumor growth and identify a pivotal role for these cells in maintaining a population of perivascular mesenchymal cells that express α-smooth muscle actin and phenotypically resemble pericytes. Using photolabeling techniques, we show that mesenchymal cells maintain their prevalence in the growing tumor through proliferation and uncover a role for Lyve-1(+) TAMs in orchestrating a selective platelet-derived growth factor–CC–dependent expansion of the perivascular mesenchymal population, creating a proangiogenic niche. This study highlights the inter-reliance of the immune and nonimmune stromal network that supports cancer progression and provides therapeutic opportunities for tackling the disease.
format Online
Article
Text
id pubmed-8565907
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher American Association for the Advancement of Science
record_format MEDLINE/PubMed
spelling pubmed-85659072021-11-17 Macrophages orchestrate the expansion of a proangiogenic perivascular niche during cancer progression Opzoomer, James W. Anstee, Joanne E. Dean, Isaac Hill, Emily J. Bouybayoune, Ihssane Caron, Jonathan Muliaditan, Tamara Gordon, Peter Sosnowska, Dominika Nuamah, Rosamond Pinder, Sarah E. Ng, Tony Dazzi, Francesco Kordasti, Shahram Withers, David R. Lawrence, Toby Arnold, James N. Sci Adv Biomedicine and Life Sciences Tumor-associated macrophages (TAMs) are a highly plastic stromal cell type that support cancer progression. Using single-cell RNA sequencing of TAMs from a spontaneous murine model of mammary adenocarcinoma (MMTV-PyMT), we characterize a subset of these cells expressing lymphatic vessel endothelial hyaluronic acid receptor 1 (Lyve-1) that spatially reside proximal to blood vasculature. We demonstrate that Lyve-1(+) TAMs support tumor growth and identify a pivotal role for these cells in maintaining a population of perivascular mesenchymal cells that express α-smooth muscle actin and phenotypically resemble pericytes. Using photolabeling techniques, we show that mesenchymal cells maintain their prevalence in the growing tumor through proliferation and uncover a role for Lyve-1(+) TAMs in orchestrating a selective platelet-derived growth factor–CC–dependent expansion of the perivascular mesenchymal population, creating a proangiogenic niche. This study highlights the inter-reliance of the immune and nonimmune stromal network that supports cancer progression and provides therapeutic opportunities for tackling the disease. American Association for the Advancement of Science 2021-11-03 /pmc/articles/PMC8565907/ /pubmed/34730997 http://dx.doi.org/10.1126/sciadv.abg9518 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Opzoomer, James W.
Anstee, Joanne E.
Dean, Isaac
Hill, Emily J.
Bouybayoune, Ihssane
Caron, Jonathan
Muliaditan, Tamara
Gordon, Peter
Sosnowska, Dominika
Nuamah, Rosamond
Pinder, Sarah E.
Ng, Tony
Dazzi, Francesco
Kordasti, Shahram
Withers, David R.
Lawrence, Toby
Arnold, James N.
Macrophages orchestrate the expansion of a proangiogenic perivascular niche during cancer progression
title Macrophages orchestrate the expansion of a proangiogenic perivascular niche during cancer progression
title_full Macrophages orchestrate the expansion of a proangiogenic perivascular niche during cancer progression
title_fullStr Macrophages orchestrate the expansion of a proangiogenic perivascular niche during cancer progression
title_full_unstemmed Macrophages orchestrate the expansion of a proangiogenic perivascular niche during cancer progression
title_short Macrophages orchestrate the expansion of a proangiogenic perivascular niche during cancer progression
title_sort macrophages orchestrate the expansion of a proangiogenic perivascular niche during cancer progression
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8565907/
https://www.ncbi.nlm.nih.gov/pubmed/34730997
http://dx.doi.org/10.1126/sciadv.abg9518
work_keys_str_mv AT opzoomerjamesw macrophagesorchestratetheexpansionofaproangiogenicperivascularnicheduringcancerprogression
AT ansteejoannee macrophagesorchestratetheexpansionofaproangiogenicperivascularnicheduringcancerprogression
AT deanisaac macrophagesorchestratetheexpansionofaproangiogenicperivascularnicheduringcancerprogression
AT hillemilyj macrophagesorchestratetheexpansionofaproangiogenicperivascularnicheduringcancerprogression
AT bouybayouneihssane macrophagesorchestratetheexpansionofaproangiogenicperivascularnicheduringcancerprogression
AT caronjonathan macrophagesorchestratetheexpansionofaproangiogenicperivascularnicheduringcancerprogression
AT muliaditantamara macrophagesorchestratetheexpansionofaproangiogenicperivascularnicheduringcancerprogression
AT gordonpeter macrophagesorchestratetheexpansionofaproangiogenicperivascularnicheduringcancerprogression
AT sosnowskadominika macrophagesorchestratetheexpansionofaproangiogenicperivascularnicheduringcancerprogression
AT nuamahrosamond macrophagesorchestratetheexpansionofaproangiogenicperivascularnicheduringcancerprogression
AT pindersarahe macrophagesorchestratetheexpansionofaproangiogenicperivascularnicheduringcancerprogression
AT ngtony macrophagesorchestratetheexpansionofaproangiogenicperivascularnicheduringcancerprogression
AT dazzifrancesco macrophagesorchestratetheexpansionofaproangiogenicperivascularnicheduringcancerprogression
AT kordastishahram macrophagesorchestratetheexpansionofaproangiogenicperivascularnicheduringcancerprogression
AT withersdavidr macrophagesorchestratetheexpansionofaproangiogenicperivascularnicheduringcancerprogression
AT lawrencetoby macrophagesorchestratetheexpansionofaproangiogenicperivascularnicheduringcancerprogression
AT arnoldjamesn macrophagesorchestratetheexpansionofaproangiogenicperivascularnicheduringcancerprogression