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Single metal-organic framework–embedded nanopit arrays: A new way to control neural stem cell differentiation
Stable and continuous supply of essential biomolecules is critical to mimic in vivo microenvironments wherein spontaneous generation of various cell types occurs. Here, we report a new platform that enables highly efficient neuronal cell generation of neural stem cells using single metal-organic fra...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9020781/ https://www.ncbi.nlm.nih.gov/pubmed/35442746 http://dx.doi.org/10.1126/sciadv.abj7736 |
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author | Cho, Yeon-Woo Jee, Seohyeon Suhito, Intan Rosalina Lee, Jeong-Hyeon Park, Chun Gwon Choi, Kyung Min Kim, Tae-Hyung |
author_facet | Cho, Yeon-Woo Jee, Seohyeon Suhito, Intan Rosalina Lee, Jeong-Hyeon Park, Chun Gwon Choi, Kyung Min Kim, Tae-Hyung |
author_sort | Cho, Yeon-Woo |
collection | PubMed |
description | Stable and continuous supply of essential biomolecules is critical to mimic in vivo microenvironments wherein spontaneous generation of various cell types occurs. Here, we report a new platform that enables highly efficient neuronal cell generation of neural stem cells using single metal-organic framework (MOF) nanoparticle–embedded nanopit arrays (SMENA). By optimizing the physical parameters of homogeneous periodic nanopatterns, each nanopit can confine single nMOFs (UiO-67) that are specifically designed for long-term storage and release of retinoic acid (RA). The SMENA platform successfully inhibited physical interaction with cells, which contributed to remarkable stability of the nMOF (RA⊂UiO-67) structure without inducing nanoparticle-mediated toxicity issues. Owing to the continuous and long-term supply of RA, the neural stem cells showed enhanced mRNA expressions of various neurogenesis-related activities. The developed SMENA platform can be applied to other stem cell sources and differentiation lineages and is therefore useful for various stem cell–based regenerative therapies. |
format | Online Article Text |
id | pubmed-9020781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-90207812022-05-03 Single metal-organic framework–embedded nanopit arrays: A new way to control neural stem cell differentiation Cho, Yeon-Woo Jee, Seohyeon Suhito, Intan Rosalina Lee, Jeong-Hyeon Park, Chun Gwon Choi, Kyung Min Kim, Tae-Hyung Sci Adv Neuroscience Stable and continuous supply of essential biomolecules is critical to mimic in vivo microenvironments wherein spontaneous generation of various cell types occurs. Here, we report a new platform that enables highly efficient neuronal cell generation of neural stem cells using single metal-organic framework (MOF) nanoparticle–embedded nanopit arrays (SMENA). By optimizing the physical parameters of homogeneous periodic nanopatterns, each nanopit can confine single nMOFs (UiO-67) that are specifically designed for long-term storage and release of retinoic acid (RA). The SMENA platform successfully inhibited physical interaction with cells, which contributed to remarkable stability of the nMOF (RA⊂UiO-67) structure without inducing nanoparticle-mediated toxicity issues. Owing to the continuous and long-term supply of RA, the neural stem cells showed enhanced mRNA expressions of various neurogenesis-related activities. The developed SMENA platform can be applied to other stem cell sources and differentiation lineages and is therefore useful for various stem cell–based regenerative therapies. American Association for the Advancement of Science 2022-04-20 /pmc/articles/PMC9020781/ /pubmed/35442746 http://dx.doi.org/10.1126/sciadv.abj7736 Text en Copyright © 2022 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 NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Neuroscience Cho, Yeon-Woo Jee, Seohyeon Suhito, Intan Rosalina Lee, Jeong-Hyeon Park, Chun Gwon Choi, Kyung Min Kim, Tae-Hyung Single metal-organic framework–embedded nanopit arrays: A new way to control neural stem cell differentiation |
title | Single metal-organic framework–embedded nanopit arrays: A new way to control neural stem cell differentiation |
title_full | Single metal-organic framework–embedded nanopit arrays: A new way to control neural stem cell differentiation |
title_fullStr | Single metal-organic framework–embedded nanopit arrays: A new way to control neural stem cell differentiation |
title_full_unstemmed | Single metal-organic framework–embedded nanopit arrays: A new way to control neural stem cell differentiation |
title_short | Single metal-organic framework–embedded nanopit arrays: A new way to control neural stem cell differentiation |
title_sort | single metal-organic framework–embedded nanopit arrays: a new way to control neural stem cell differentiation |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9020781/ https://www.ncbi.nlm.nih.gov/pubmed/35442746 http://dx.doi.org/10.1126/sciadv.abj7736 |
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