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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...

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Autores principales: Sandhurst, Eric S., Jaswandkar, Sharad V., Kundu, Krishna, Katti, Dinesh R., Katti, Kalpana S., Sun, Hongli, Engebretson, Daniel, Francis, Kevin R.
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
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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.
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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
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