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Programming of Multicellular Patterning with Mechano‐Chemically Microstructured Cell Niches
Multicellular patterning of stem‐cell‐derived tissue models is commonly achieved via self‐organizing activities triggered by exogenous morphogenetic stimuli. However, such tissue models are prone to stochastic behavior, limiting the reproducibility of cellular composition and forming non‐physiologic...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10214222/ https://www.ncbi.nlm.nih.gov/pubmed/36998105 http://dx.doi.org/10.1002/advs.202204741 |
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author | Newman, Peter L. H. Yip, Queenie Osteil, Pierre Anderson, Tim A. Sun, Jane Q. J. Kempe, Daryan Biro, Maté Shin, Jae‐Won Tam, Patrick P. L. Zreiqat, Hala |
author_facet | Newman, Peter L. H. Yip, Queenie Osteil, Pierre Anderson, Tim A. Sun, Jane Q. J. Kempe, Daryan Biro, Maté Shin, Jae‐Won Tam, Patrick P. L. Zreiqat, Hala |
author_sort | Newman, Peter L. H. |
collection | PubMed |
description | Multicellular patterning of stem‐cell‐derived tissue models is commonly achieved via self‐organizing activities triggered by exogenous morphogenetic stimuli. However, such tissue models are prone to stochastic behavior, limiting the reproducibility of cellular composition and forming non‐physiological architectures. To enhance multicellular patterning in stem cell‐derived tissues, a method for creating complex tissue microenvironments endowed with programmable multimodal mechano‐chemical cues, including conjugated peptides, proteins, morphogens, and Young's moduli defined over a range of stiffnesses is developed. The ability of these cues to spatially guide tissue patterning processes, including mechanosensing and the biochemically driven differentiation of selected cell types, is demonstrated. By rationally designing niches, the authors engineered a bone‐fat assembly from stromal mesenchyme cells and regionalized germ layer tissues from pluripotent stem cells. Through defined niche‐material interactions, mechano‐chemically microstructured niches enable the spatial programming of tissue patterning processes. Mechano‐chemically microstructured cell niches thereby offer an entry point for enhancing the organization and composition of engineered tissues, potentiating structures that better recapitulate their native counterparts. |
format | Online Article Text |
id | pubmed-10214222 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102142222023-05-27 Programming of Multicellular Patterning with Mechano‐Chemically Microstructured Cell Niches Newman, Peter L. H. Yip, Queenie Osteil, Pierre Anderson, Tim A. Sun, Jane Q. J. Kempe, Daryan Biro, Maté Shin, Jae‐Won Tam, Patrick P. L. Zreiqat, Hala Adv Sci (Weinh) Research Articles Multicellular patterning of stem‐cell‐derived tissue models is commonly achieved via self‐organizing activities triggered by exogenous morphogenetic stimuli. However, such tissue models are prone to stochastic behavior, limiting the reproducibility of cellular composition and forming non‐physiological architectures. To enhance multicellular patterning in stem cell‐derived tissues, a method for creating complex tissue microenvironments endowed with programmable multimodal mechano‐chemical cues, including conjugated peptides, proteins, morphogens, and Young's moduli defined over a range of stiffnesses is developed. The ability of these cues to spatially guide tissue patterning processes, including mechanosensing and the biochemically driven differentiation of selected cell types, is demonstrated. By rationally designing niches, the authors engineered a bone‐fat assembly from stromal mesenchyme cells and regionalized germ layer tissues from pluripotent stem cells. Through defined niche‐material interactions, mechano‐chemically microstructured niches enable the spatial programming of tissue patterning processes. Mechano‐chemically microstructured cell niches thereby offer an entry point for enhancing the organization and composition of engineered tissues, potentiating structures that better recapitulate their native counterparts. John Wiley and Sons Inc. 2023-03-30 /pmc/articles/PMC10214222/ /pubmed/36998105 http://dx.doi.org/10.1002/advs.202204741 Text en © 2023 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Newman, Peter L. H. Yip, Queenie Osteil, Pierre Anderson, Tim A. Sun, Jane Q. J. Kempe, Daryan Biro, Maté Shin, Jae‐Won Tam, Patrick P. L. Zreiqat, Hala Programming of Multicellular Patterning with Mechano‐Chemically Microstructured Cell Niches |
title | Programming of Multicellular Patterning with Mechano‐Chemically Microstructured Cell Niches |
title_full | Programming of Multicellular Patterning with Mechano‐Chemically Microstructured Cell Niches |
title_fullStr | Programming of Multicellular Patterning with Mechano‐Chemically Microstructured Cell Niches |
title_full_unstemmed | Programming of Multicellular Patterning with Mechano‐Chemically Microstructured Cell Niches |
title_short | Programming of Multicellular Patterning with Mechano‐Chemically Microstructured Cell Niches |
title_sort | programming of multicellular patterning with mechano‐chemically microstructured cell niches |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10214222/ https://www.ncbi.nlm.nih.gov/pubmed/36998105 http://dx.doi.org/10.1002/advs.202204741 |
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