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Omental macrophages secrete chemokine ligands that promote ovarian cancer colonization of the omentum via CCR1
The omentum is the most common site of ovarian cancer metastasis. Immune cell clusters called milky spots are found throughout the omentum. It is however unknown if these immune cells contribute to ovarian cancer metastasis. Here we report that omental macrophages promote the migration and colonizat...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7508838/ https://www.ncbi.nlm.nih.gov/pubmed/32963283 http://dx.doi.org/10.1038/s42003-020-01246-z |
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author | Krishnan, Venkatesh Tallapragada, Supreeti Schaar, Bruce Kamat, Kalika Chanana, Anita M. Zhang, Yue Patel, Sonia Parkash, Vinita Rinker-Schaeffer, Carrie Folkins, Ann K. Rankin, Erinn B. Dorigo, Oliver |
author_facet | Krishnan, Venkatesh Tallapragada, Supreeti Schaar, Bruce Kamat, Kalika Chanana, Anita M. Zhang, Yue Patel, Sonia Parkash, Vinita Rinker-Schaeffer, Carrie Folkins, Ann K. Rankin, Erinn B. Dorigo, Oliver |
author_sort | Krishnan, Venkatesh |
collection | PubMed |
description | The omentum is the most common site of ovarian cancer metastasis. Immune cell clusters called milky spots are found throughout the omentum. It is however unknown if these immune cells contribute to ovarian cancer metastasis. Here we report that omental macrophages promote the migration and colonization of ovarian cancer cells to the omentum through the secretion of chemokine ligands that interact with chemokine receptor 1 (CCR1). We found that depletion of macrophages reduces ovarian cancer colonization of the omentum. RNA-sequencing of macrophages isolated from mouse omentum and mesenteric adipose tissue revealed a specific enrichment of chemokine ligand CCL6 in omental macrophages. CCL6 and the human homolog CCL23 were both necessary and sufficient to promote ovarian cancer migration by activating ERK1/2 and PI3K pathways. Importantly, inhibition of CCR1 reduced ovarian cancer colonization. These findings demonstrate a critical mechanism of omental macrophage induced colonization by ovarian cancer cells via CCR1 signaling. |
format | Online Article Text |
id | pubmed-7508838 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75088382020-10-08 Omental macrophages secrete chemokine ligands that promote ovarian cancer colonization of the omentum via CCR1 Krishnan, Venkatesh Tallapragada, Supreeti Schaar, Bruce Kamat, Kalika Chanana, Anita M. Zhang, Yue Patel, Sonia Parkash, Vinita Rinker-Schaeffer, Carrie Folkins, Ann K. Rankin, Erinn B. Dorigo, Oliver Commun Biol Article The omentum is the most common site of ovarian cancer metastasis. Immune cell clusters called milky spots are found throughout the omentum. It is however unknown if these immune cells contribute to ovarian cancer metastasis. Here we report that omental macrophages promote the migration and colonization of ovarian cancer cells to the omentum through the secretion of chemokine ligands that interact with chemokine receptor 1 (CCR1). We found that depletion of macrophages reduces ovarian cancer colonization of the omentum. RNA-sequencing of macrophages isolated from mouse omentum and mesenteric adipose tissue revealed a specific enrichment of chemokine ligand CCL6 in omental macrophages. CCL6 and the human homolog CCL23 were both necessary and sufficient to promote ovarian cancer migration by activating ERK1/2 and PI3K pathways. Importantly, inhibition of CCR1 reduced ovarian cancer colonization. These findings demonstrate a critical mechanism of omental macrophage induced colonization by ovarian cancer cells via CCR1 signaling. Nature Publishing Group UK 2020-09-22 /pmc/articles/PMC7508838/ /pubmed/32963283 http://dx.doi.org/10.1038/s42003-020-01246-z Text en © The Author(s) 2020 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 Krishnan, Venkatesh Tallapragada, Supreeti Schaar, Bruce Kamat, Kalika Chanana, Anita M. Zhang, Yue Patel, Sonia Parkash, Vinita Rinker-Schaeffer, Carrie Folkins, Ann K. Rankin, Erinn B. Dorigo, Oliver Omental macrophages secrete chemokine ligands that promote ovarian cancer colonization of the omentum via CCR1 |
title | Omental macrophages secrete chemokine ligands that promote ovarian cancer colonization of the omentum via CCR1 |
title_full | Omental macrophages secrete chemokine ligands that promote ovarian cancer colonization of the omentum via CCR1 |
title_fullStr | Omental macrophages secrete chemokine ligands that promote ovarian cancer colonization of the omentum via CCR1 |
title_full_unstemmed | Omental macrophages secrete chemokine ligands that promote ovarian cancer colonization of the omentum via CCR1 |
title_short | Omental macrophages secrete chemokine ligands that promote ovarian cancer colonization of the omentum via CCR1 |
title_sort | omental macrophages secrete chemokine ligands that promote ovarian cancer colonization of the omentum via ccr1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7508838/ https://www.ncbi.nlm.nih.gov/pubmed/32963283 http://dx.doi.org/10.1038/s42003-020-01246-z |
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