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Functional maturation of human neural stem cells in a 3D bioengineered brain model enriched with fetal brain-derived matrix

Brain extracellular matrix (ECM) is often overlooked in vitro brain tissue models, despite its instructive roles during development. Using developmental stage-sourced brain ECM in reproducible 3D bioengineered culture systems, we demonstrate enhanced functional differentiation of human induced neura...

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Autores principales: Sood, Disha, Cairns, Dana M., Dabbi, Jayanth M., Ramakrishnan, Charu, Deisseroth, Karl, Black, Lauren D., Santaniello, Sabato, 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/PMC6884597/
https://www.ncbi.nlm.nih.gov/pubmed/31784595
http://dx.doi.org/10.1038/s41598-019-54248-1
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author Sood, Disha
Cairns, Dana M.
Dabbi, Jayanth M.
Ramakrishnan, Charu
Deisseroth, Karl
Black, Lauren D.
Santaniello, Sabato
Kaplan, David L.
author_facet Sood, Disha
Cairns, Dana M.
Dabbi, Jayanth M.
Ramakrishnan, Charu
Deisseroth, Karl
Black, Lauren D.
Santaniello, Sabato
Kaplan, David L.
author_sort Sood, Disha
collection PubMed
description Brain extracellular matrix (ECM) is often overlooked in vitro brain tissue models, despite its instructive roles during development. Using developmental stage-sourced brain ECM in reproducible 3D bioengineered culture systems, we demonstrate enhanced functional differentiation of human induced neural stem cells (hiNSCs) into healthy neurons and astrocytes. Particularly, fetal brain tissue-derived ECM supported long-term maintenance of differentiated neurons, demonstrated by morphology, gene expression and secretome profiling. Astrocytes were evident within the second month of differentiation, and reactive astrogliosis was inhibited in brain ECM-enriched cultures when compared to unsupplemented cultures. Functional maturation of the differentiated hiNSCs within fetal ECM-enriched cultures was confirmed by calcium signaling and spectral/cluster analysis. Additionally, the study identified native biochemical cues in decellularized ECM with notable comparisons between fetal and adult brain-derived ECMs. The development of novel brain-specific biomaterials for generating mature in vitro brain models provides an important path forward for interrogation of neuron-glia interactions.
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spelling pubmed-68845972019-12-06 Functional maturation of human neural stem cells in a 3D bioengineered brain model enriched with fetal brain-derived matrix Sood, Disha Cairns, Dana M. Dabbi, Jayanth M. Ramakrishnan, Charu Deisseroth, Karl Black, Lauren D. Santaniello, Sabato Kaplan, David L. Sci Rep Article Brain extracellular matrix (ECM) is often overlooked in vitro brain tissue models, despite its instructive roles during development. Using developmental stage-sourced brain ECM in reproducible 3D bioengineered culture systems, we demonstrate enhanced functional differentiation of human induced neural stem cells (hiNSCs) into healthy neurons and astrocytes. Particularly, fetal brain tissue-derived ECM supported long-term maintenance of differentiated neurons, demonstrated by morphology, gene expression and secretome profiling. Astrocytes were evident within the second month of differentiation, and reactive astrogliosis was inhibited in brain ECM-enriched cultures when compared to unsupplemented cultures. Functional maturation of the differentiated hiNSCs within fetal ECM-enriched cultures was confirmed by calcium signaling and spectral/cluster analysis. Additionally, the study identified native biochemical cues in decellularized ECM with notable comparisons between fetal and adult brain-derived ECMs. The development of novel brain-specific biomaterials for generating mature in vitro brain models provides an important path forward for interrogation of neuron-glia interactions. Nature Publishing Group UK 2019-11-29 /pmc/articles/PMC6884597/ /pubmed/31784595 http://dx.doi.org/10.1038/s41598-019-54248-1 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
Cairns, Dana M.
Dabbi, Jayanth M.
Ramakrishnan, Charu
Deisseroth, Karl
Black, Lauren D.
Santaniello, Sabato
Kaplan, David L.
Functional maturation of human neural stem cells in a 3D bioengineered brain model enriched with fetal brain-derived matrix
title Functional maturation of human neural stem cells in a 3D bioengineered brain model enriched with fetal brain-derived matrix
title_full Functional maturation of human neural stem cells in a 3D bioengineered brain model enriched with fetal brain-derived matrix
title_fullStr Functional maturation of human neural stem cells in a 3D bioengineered brain model enriched with fetal brain-derived matrix
title_full_unstemmed Functional maturation of human neural stem cells in a 3D bioengineered brain model enriched with fetal brain-derived matrix
title_short Functional maturation of human neural stem cells in a 3D bioengineered brain model enriched with fetal brain-derived matrix
title_sort functional maturation of human neural stem cells in a 3d bioengineered brain model enriched with fetal brain-derived matrix
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6884597/
https://www.ncbi.nlm.nih.gov/pubmed/31784595
http://dx.doi.org/10.1038/s41598-019-54248-1
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