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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...

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Autores principales: McCoy, Michael G., Nyanyo, Dennis, Hung, Carol K., Goerger, Julian Palacios, R. Zipfel, Warren, Williams, Rebecca M., Nishimura, Nozomi, Fischbach, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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.
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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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