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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
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.
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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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