Cargando…
Nanoarchitectonics of a Microsphere-Based Scaffold for Modeling Neurodevelopment and Neurological Disease
[Image: see text] Three-dimensional cellular constructs derived from pluripotent stem cells allow the ex vivo study of neurodevelopment and neurological disease within a spatially organized model. However, the robustness and utility of three-dimensional models is impacted by tissue self-organization...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8865216/ https://www.ncbi.nlm.nih.gov/pubmed/35045249 http://dx.doi.org/10.1021/acsabm.1c01012 |
_version_ | 1784655607277551616 |
---|---|
author | Sandhurst, Eric S. Jaswandkar, Sharad V. Kundu, Krishna Katti, Dinesh R. Katti, Kalpana S. Sun, Hongli Engebretson, Daniel Francis, Kevin R. |
author_facet | Sandhurst, Eric S. Jaswandkar, Sharad V. Kundu, Krishna Katti, Dinesh R. Katti, Kalpana S. Sun, Hongli Engebretson, Daniel Francis, Kevin R. |
author_sort | Sandhurst, Eric S. |
collection | PubMed |
description | [Image: see text] Three-dimensional cellular constructs derived from pluripotent stem cells allow the ex vivo study of neurodevelopment and neurological disease within a spatially organized model. However, the robustness and utility of three-dimensional models is impacted by tissue self-organization, size limitations, nutrient supply, and heterogeneity. In this work, we have utilized the principles of nanoarchitectonics to create a multifunctional polymer/bioceramic composite microsphere system for stem cell culture and differentiation in a chemically defined microenvironment. Microspheres could be customized to produce three-dimensional structures of defined size (ranging from >100 to <350 μm) with lower mechanical properties compared with a thin film. Furthermore, the microspheres softened in solution, approaching more tissue-like mechanical properties over time. With neural stem cells (NSCs) derived from human induced pluripotent stem cells, microsphere-cultured NSCs were able to utilize multiple substrates to promote cell adhesion and proliferation. Prolonged culture of NSC-bound microspheres under differentiating conditions allowed the formation of both neural and glial cell types from control and patient-derived stem cell models. Human NSCs and differentiated neurons could also be cocultured with astrocytes and human umbilical vein endothelial cells, demonstrating application for tissue-engineered modeling of development and human disease. We further demonstrated that microspheres allow the loading and sustained release of multiple recombinant proteins to support cellular maintenance and differentiation. While previous work has principally utilized self-organizing models or protein-rich hydrogels for neural culture, the three-dimensional matrix developed here through nanoarchitectonics represents a chemically defined and robust alternative for the in vitro study of neurodevelopment and nervous system disorders. |
format | Online Article Text |
id | pubmed-8865216 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-88652162023-01-19 Nanoarchitectonics of a Microsphere-Based Scaffold for Modeling Neurodevelopment and Neurological Disease Sandhurst, Eric S. Jaswandkar, Sharad V. Kundu, Krishna Katti, Dinesh R. Katti, Kalpana S. Sun, Hongli Engebretson, Daniel Francis, Kevin R. ACS Appl Bio Mater [Image: see text] Three-dimensional cellular constructs derived from pluripotent stem cells allow the ex vivo study of neurodevelopment and neurological disease within a spatially organized model. However, the robustness and utility of three-dimensional models is impacted by tissue self-organization, size limitations, nutrient supply, and heterogeneity. In this work, we have utilized the principles of nanoarchitectonics to create a multifunctional polymer/bioceramic composite microsphere system for stem cell culture and differentiation in a chemically defined microenvironment. Microspheres could be customized to produce three-dimensional structures of defined size (ranging from >100 to <350 μm) with lower mechanical properties compared with a thin film. Furthermore, the microspheres softened in solution, approaching more tissue-like mechanical properties over time. With neural stem cells (NSCs) derived from human induced pluripotent stem cells, microsphere-cultured NSCs were able to utilize multiple substrates to promote cell adhesion and proliferation. Prolonged culture of NSC-bound microspheres under differentiating conditions allowed the formation of both neural and glial cell types from control and patient-derived stem cell models. Human NSCs and differentiated neurons could also be cocultured with astrocytes and human umbilical vein endothelial cells, demonstrating application for tissue-engineered modeling of development and human disease. We further demonstrated that microspheres allow the loading and sustained release of multiple recombinant proteins to support cellular maintenance and differentiation. While previous work has principally utilized self-organizing models or protein-rich hydrogels for neural culture, the three-dimensional matrix developed here through nanoarchitectonics represents a chemically defined and robust alternative for the in vitro study of neurodevelopment and nervous system disorders. American Chemical Society 2022-01-19 2022-02-21 /pmc/articles/PMC8865216/ /pubmed/35045249 http://dx.doi.org/10.1021/acsabm.1c01012 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Sandhurst, Eric S. Jaswandkar, Sharad V. Kundu, Krishna Katti, Dinesh R. Katti, Kalpana S. Sun, Hongli Engebretson, Daniel Francis, Kevin R. Nanoarchitectonics of a Microsphere-Based Scaffold for Modeling Neurodevelopment and Neurological Disease |
title | Nanoarchitectonics of a Microsphere-Based Scaffold
for Modeling Neurodevelopment and Neurological Disease |
title_full | Nanoarchitectonics of a Microsphere-Based Scaffold
for Modeling Neurodevelopment and Neurological Disease |
title_fullStr | Nanoarchitectonics of a Microsphere-Based Scaffold
for Modeling Neurodevelopment and Neurological Disease |
title_full_unstemmed | Nanoarchitectonics of a Microsphere-Based Scaffold
for Modeling Neurodevelopment and Neurological Disease |
title_short | Nanoarchitectonics of a Microsphere-Based Scaffold
for Modeling Neurodevelopment and Neurological Disease |
title_sort | nanoarchitectonics of a microsphere-based scaffold
for modeling neurodevelopment and neurological disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8865216/ https://www.ncbi.nlm.nih.gov/pubmed/35045249 http://dx.doi.org/10.1021/acsabm.1c01012 |
work_keys_str_mv | AT sandhursterics nanoarchitectonicsofamicrospherebasedscaffoldformodelingneurodevelopmentandneurologicaldisease AT jaswandkarsharadv nanoarchitectonicsofamicrospherebasedscaffoldformodelingneurodevelopmentandneurologicaldisease AT kundukrishna nanoarchitectonicsofamicrospherebasedscaffoldformodelingneurodevelopmentandneurologicaldisease AT kattidineshr nanoarchitectonicsofamicrospherebasedscaffoldformodelingneurodevelopmentandneurologicaldisease AT kattikalpanas nanoarchitectonicsofamicrospherebasedscaffoldformodelingneurodevelopmentandneurologicaldisease AT sunhongli nanoarchitectonicsofamicrospherebasedscaffoldformodelingneurodevelopmentandneurologicaldisease AT engebretsondaniel nanoarchitectonicsofamicrospherebasedscaffoldformodelingneurodevelopmentandneurologicaldisease AT franciskevinr nanoarchitectonicsofamicrospherebasedscaffoldformodelingneurodevelopmentandneurologicaldisease |