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Endothelial cells promote 3D invasion of GBM by IL-8-dependent induction of cancer stem cell properties
Rapid growth and perivascular invasion are hallmarks of glioblastoma (GBM) that have been attributed to the presence of cancer stem-like cells (CSCs) and their association with the perivascular niche. However, the mechanisms by which the perivascular niche regulates GBM invasion and CSCs remain poor...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6588602/ https://www.ncbi.nlm.nih.gov/pubmed/31227783 http://dx.doi.org/10.1038/s41598-019-45535-y |
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author | McCoy, Michael G. Nyanyo, Dennis Hung, Carol K. Goerger, Julian Palacios R. Zipfel, Warren Williams, Rebecca M. Nishimura, Nozomi Fischbach, Claudia |
author_facet | McCoy, Michael G. Nyanyo, Dennis Hung, Carol K. Goerger, Julian Palacios R. Zipfel, Warren Williams, Rebecca M. Nishimura, Nozomi Fischbach, Claudia |
author_sort | McCoy, Michael G. |
collection | PubMed |
description | Rapid growth and perivascular invasion are hallmarks of glioblastoma (GBM) that have been attributed to the presence of cancer stem-like cells (CSCs) and their association with the perivascular niche. However, the mechanisms by which the perivascular niche regulates GBM invasion and CSCs remain poorly understood due in part to a lack of relevant model systems. To simulate perivascular niche conditions and analyze consequential changes of GBM growth and invasion, patient-derived GBM spheroids were co-cultured with brain endothelial cells (ECs) in microfabricated collagen gels. Integrating these systems with 3D imaging and biochemical assays revealed that ECs increase GBM invasiveness and growth through interleukin-8 (IL-8)-mediated enrichment of CSCs. Blockade of IL-8 inhibited these effects in GBM-EC co-cultures, while IL-8 supplementation increased CSC-mediated growth and invasion in GBM-monocultures. Experiments in mice confirmed that ECs and IL-8 stimulate intracranial tumor growth and invasion in vivo. Collectively, perivascular niche conditions promote GBM growth and invasion by increasing CSC frequency, and IL-8 may be explored clinically to inhibit these interactions. |
format | Online Article Text |
id | pubmed-6588602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65886022019-06-28 Endothelial cells promote 3D invasion of GBM by IL-8-dependent induction of cancer stem cell properties McCoy, Michael G. Nyanyo, Dennis Hung, Carol K. Goerger, Julian Palacios R. Zipfel, Warren Williams, Rebecca M. Nishimura, Nozomi Fischbach, Claudia Sci Rep Article Rapid growth and perivascular invasion are hallmarks of glioblastoma (GBM) that have been attributed to the presence of cancer stem-like cells (CSCs) and their association with the perivascular niche. However, the mechanisms by which the perivascular niche regulates GBM invasion and CSCs remain poorly understood due in part to a lack of relevant model systems. To simulate perivascular niche conditions and analyze consequential changes of GBM growth and invasion, patient-derived GBM spheroids were co-cultured with brain endothelial cells (ECs) in microfabricated collagen gels. Integrating these systems with 3D imaging and biochemical assays revealed that ECs increase GBM invasiveness and growth through interleukin-8 (IL-8)-mediated enrichment of CSCs. Blockade of IL-8 inhibited these effects in GBM-EC co-cultures, while IL-8 supplementation increased CSC-mediated growth and invasion in GBM-monocultures. Experiments in mice confirmed that ECs and IL-8 stimulate intracranial tumor growth and invasion in vivo. Collectively, perivascular niche conditions promote GBM growth and invasion by increasing CSC frequency, and IL-8 may be explored clinically to inhibit these interactions. Nature Publishing Group UK 2019-06-21 /pmc/articles/PMC6588602/ /pubmed/31227783 http://dx.doi.org/10.1038/s41598-019-45535-y 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 McCoy, Michael G. Nyanyo, Dennis Hung, Carol K. Goerger, Julian Palacios R. Zipfel, Warren Williams, Rebecca M. Nishimura, Nozomi Fischbach, Claudia Endothelial cells promote 3D invasion of GBM by IL-8-dependent induction of cancer stem cell properties |
title | Endothelial cells promote 3D invasion of GBM by IL-8-dependent induction of cancer stem cell properties |
title_full | Endothelial cells promote 3D invasion of GBM by IL-8-dependent induction of cancer stem cell properties |
title_fullStr | Endothelial cells promote 3D invasion of GBM by IL-8-dependent induction of cancer stem cell properties |
title_full_unstemmed | Endothelial cells promote 3D invasion of GBM by IL-8-dependent induction of cancer stem cell properties |
title_short | Endothelial cells promote 3D invasion of GBM by IL-8-dependent induction of cancer stem cell properties |
title_sort | endothelial cells promote 3d invasion of gbm by il-8-dependent induction of cancer stem cell properties |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6588602/ https://www.ncbi.nlm.nih.gov/pubmed/31227783 http://dx.doi.org/10.1038/s41598-019-45535-y |
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