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3D extracellular matrix microenvironment in bioengineered tissue models of primary pediatric and adult brain tumors

Dynamic alterations in the unique brain extracellular matrix (ECM) are involved in malignant brain tumors. Yet studies of brain ECM roles in tumor cell behavior have been difficult due to lack of access to the human brain. We present a tunable 3D bioengineered brain tissue platform by integrating mi...

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Autores principales: Sood, Disha, Tang-Schomer, Min, Pouli, Dimitra, Mizzoni, Craig, Raia, Nicole, Tai, Albert, Arkun, Knarik, Wu, Julian, Black, Lauren D., Scheffler, Bjorn, Georgakoudi, Irene, Steindler, Dennis A., Kaplan, David L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6778192/
https://www.ncbi.nlm.nih.gov/pubmed/31586101
http://dx.doi.org/10.1038/s41467-019-12420-1
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author Sood, Disha
Tang-Schomer, Min
Pouli, Dimitra
Mizzoni, Craig
Raia, Nicole
Tai, Albert
Arkun, Knarik
Wu, Julian
Black, Lauren D.
Scheffler, Bjorn
Georgakoudi, Irene
Steindler, Dennis A.
Kaplan, David L.
author_facet Sood, Disha
Tang-Schomer, Min
Pouli, Dimitra
Mizzoni, Craig
Raia, Nicole
Tai, Albert
Arkun, Knarik
Wu, Julian
Black, Lauren D.
Scheffler, Bjorn
Georgakoudi, Irene
Steindler, Dennis A.
Kaplan, David L.
author_sort Sood, Disha
collection PubMed
description Dynamic alterations in the unique brain extracellular matrix (ECM) are involved in malignant brain tumors. Yet studies of brain ECM roles in tumor cell behavior have been difficult due to lack of access to the human brain. We present a tunable 3D bioengineered brain tissue platform by integrating microenvironmental cues of native brain-derived ECMs and live imaging to systematically evaluate patient-derived brain tumor responses. Using pediatric ependymoma and adult glioblastoma as examples, the 3D brain ECM-containing microenvironment with a balance of cell-cell and cell-matrix interactions supports distinctive phenotypes associated with tumor type-specific and ECM-dependent patterns in the tumor cells’ transcriptomic and release profiles. Label-free metabolic imaging of the composite model structure identifies metabolically distinct sub-populations within a tumor type and captures extracellular lipid-containing droplets with potential implications in drug response. The versatile bioengineered 3D tumor tissue system sets the stage for mechanistic studies deciphering microenvironmental role in brain tumor progression.
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spelling pubmed-67781922019-10-07 3D extracellular matrix microenvironment in bioengineered tissue models of primary pediatric and adult brain tumors Sood, Disha Tang-Schomer, Min Pouli, Dimitra Mizzoni, Craig Raia, Nicole Tai, Albert Arkun, Knarik Wu, Julian Black, Lauren D. Scheffler, Bjorn Georgakoudi, Irene Steindler, Dennis A. Kaplan, David L. Nat Commun Article Dynamic alterations in the unique brain extracellular matrix (ECM) are involved in malignant brain tumors. Yet studies of brain ECM roles in tumor cell behavior have been difficult due to lack of access to the human brain. We present a tunable 3D bioengineered brain tissue platform by integrating microenvironmental cues of native brain-derived ECMs and live imaging to systematically evaluate patient-derived brain tumor responses. Using pediatric ependymoma and adult glioblastoma as examples, the 3D brain ECM-containing microenvironment with a balance of cell-cell and cell-matrix interactions supports distinctive phenotypes associated with tumor type-specific and ECM-dependent patterns in the tumor cells’ transcriptomic and release profiles. Label-free metabolic imaging of the composite model structure identifies metabolically distinct sub-populations within a tumor type and captures extracellular lipid-containing droplets with potential implications in drug response. The versatile bioengineered 3D tumor tissue system sets the stage for mechanistic studies deciphering microenvironmental role in brain tumor progression. Nature Publishing Group UK 2019-10-04 /pmc/articles/PMC6778192/ /pubmed/31586101 http://dx.doi.org/10.1038/s41467-019-12420-1 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
Sood, Disha
Tang-Schomer, Min
Pouli, Dimitra
Mizzoni, Craig
Raia, Nicole
Tai, Albert
Arkun, Knarik
Wu, Julian
Black, Lauren D.
Scheffler, Bjorn
Georgakoudi, Irene
Steindler, Dennis A.
Kaplan, David L.
3D extracellular matrix microenvironment in bioengineered tissue models of primary pediatric and adult brain tumors
title 3D extracellular matrix microenvironment in bioengineered tissue models of primary pediatric and adult brain tumors
title_full 3D extracellular matrix microenvironment in bioengineered tissue models of primary pediatric and adult brain tumors
title_fullStr 3D extracellular matrix microenvironment in bioengineered tissue models of primary pediatric and adult brain tumors
title_full_unstemmed 3D extracellular matrix microenvironment in bioengineered tissue models of primary pediatric and adult brain tumors
title_short 3D extracellular matrix microenvironment in bioengineered tissue models of primary pediatric and adult brain tumors
title_sort 3d extracellular matrix microenvironment in bioengineered tissue models of primary pediatric and adult brain tumors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6778192/
https://www.ncbi.nlm.nih.gov/pubmed/31586101
http://dx.doi.org/10.1038/s41467-019-12420-1
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