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Bioengineered perfused human brain microvascular networks enhance neural progenitor cell survival, neurogenesis, and maturation
Neural progenitor cells (NPCs) have the capability to self-renew and differentiate into neurons and glial cells. In the adult brain, NPCs are found near brain microvascular networks (BMVNs) in specialized microenvironments called the neurovascular niche (NVN). Although several in vitro NVN models ha...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10171804/ https://www.ncbi.nlm.nih.gov/pubmed/37163593 http://dx.doi.org/10.1126/sciadv.aaz9499 |
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author | Winkelman, Max A. Dai, Guohao |
author_facet | Winkelman, Max A. Dai, Guohao |
author_sort | Winkelman, Max A. |
collection | PubMed |
description | Neural progenitor cells (NPCs) have the capability to self-renew and differentiate into neurons and glial cells. In the adult brain, NPCs are found near brain microvascular networks (BMVNs) in specialized microenvironments called the neurovascular niche (NVN). Although several in vitro NVN models have been previously reported, most do not properly recapitulate the intimate cellular interactions between NPCs and perfused brain microvessels. Here, we developed perfused BMVNs composed of primary human brain endothelial cells, pericytes, and astrocytes within microfluidic devices. When induced pluripotent stem cell–derived NPCs were introduced into BMVNs, we found that NPC survival, neurogenesis, and maturation were enhanced. The application of flow during BMVN coculture was also beneficial for neuron differentiation. Collectively, our work highlighted the important role of BMVNs and flow in NPC self-renewal and neurogenesis, as well as demonstrated our model’s potential to study the biological and physical interactions of human NVN in vitro. |
format | Online Article Text |
id | pubmed-10171804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-101718042023-05-11 Bioengineered perfused human brain microvascular networks enhance neural progenitor cell survival, neurogenesis, and maturation Winkelman, Max A. Dai, Guohao Sci Adv Biomedicine and Life Sciences Neural progenitor cells (NPCs) have the capability to self-renew and differentiate into neurons and glial cells. In the adult brain, NPCs are found near brain microvascular networks (BMVNs) in specialized microenvironments called the neurovascular niche (NVN). Although several in vitro NVN models have been previously reported, most do not properly recapitulate the intimate cellular interactions between NPCs and perfused brain microvessels. Here, we developed perfused BMVNs composed of primary human brain endothelial cells, pericytes, and astrocytes within microfluidic devices. When induced pluripotent stem cell–derived NPCs were introduced into BMVNs, we found that NPC survival, neurogenesis, and maturation were enhanced. The application of flow during BMVN coculture was also beneficial for neuron differentiation. Collectively, our work highlighted the important role of BMVNs and flow in NPC self-renewal and neurogenesis, as well as demonstrated our model’s potential to study the biological and physical interactions of human NVN in vitro. American Association for the Advancement of Science 2023-05-10 /pmc/articles/PMC10171804/ /pubmed/37163593 http://dx.doi.org/10.1126/sciadv.aaz9499 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Winkelman, Max A. Dai, Guohao Bioengineered perfused human brain microvascular networks enhance neural progenitor cell survival, neurogenesis, and maturation |
title | Bioengineered perfused human brain microvascular networks enhance neural progenitor cell survival, neurogenesis, and maturation |
title_full | Bioengineered perfused human brain microvascular networks enhance neural progenitor cell survival, neurogenesis, and maturation |
title_fullStr | Bioengineered perfused human brain microvascular networks enhance neural progenitor cell survival, neurogenesis, and maturation |
title_full_unstemmed | Bioengineered perfused human brain microvascular networks enhance neural progenitor cell survival, neurogenesis, and maturation |
title_short | Bioengineered perfused human brain microvascular networks enhance neural progenitor cell survival, neurogenesis, and maturation |
title_sort | bioengineered perfused human brain microvascular networks enhance neural progenitor cell survival, neurogenesis, and maturation |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10171804/ https://www.ncbi.nlm.nih.gov/pubmed/37163593 http://dx.doi.org/10.1126/sciadv.aaz9499 |
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