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Harnessing conserved signaling and metabolic pathways to enhance the maturation of functional engineered tissues

The development of induced-pluripotent stem cell (iPSC)-derived cell types offers promise for basic science, drug testing, disease modeling, personalized medicine, and translatable cell therapies across many tissue types. However, in practice many iPSC-derived cells have presented as immature in phy...

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Autores principales: Callaghan, Neal I., Durland, Lauren J., Ireland, Ronald G., Santerre, J. Paul, Simmons, Craig A., Davenport Huyer, Locke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9440900/
https://www.ncbi.nlm.nih.gov/pubmed/36057642
http://dx.doi.org/10.1038/s41536-022-00246-3
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author Callaghan, Neal I.
Durland, Lauren J.
Ireland, Ronald G.
Santerre, J. Paul
Simmons, Craig A.
Davenport Huyer, Locke
author_facet Callaghan, Neal I.
Durland, Lauren J.
Ireland, Ronald G.
Santerre, J. Paul
Simmons, Craig A.
Davenport Huyer, Locke
author_sort Callaghan, Neal I.
collection PubMed
description The development of induced-pluripotent stem cell (iPSC)-derived cell types offers promise for basic science, drug testing, disease modeling, personalized medicine, and translatable cell therapies across many tissue types. However, in practice many iPSC-derived cells have presented as immature in physiological function, and despite efforts to recapitulate adult maturity, most have yet to meet the necessary benchmarks for the intended tissues. Here, we summarize the available state of knowledge surrounding the physiological mechanisms underlying cell maturation in several key tissues. Common signaling consolidators, as well as potential synergies between critical signaling pathways are explored. Finally, current practices in physiologically relevant tissue engineering and experimental design are critically examined, with the goal of integrating greater decision paradigms and frameworks towards achieving efficient maturation strategies, which in turn may produce higher-valued iPSC-derived tissues.
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spelling pubmed-94409002022-09-05 Harnessing conserved signaling and metabolic pathways to enhance the maturation of functional engineered tissues Callaghan, Neal I. Durland, Lauren J. Ireland, Ronald G. Santerre, J. Paul Simmons, Craig A. Davenport Huyer, Locke NPJ Regen Med Perspective The development of induced-pluripotent stem cell (iPSC)-derived cell types offers promise for basic science, drug testing, disease modeling, personalized medicine, and translatable cell therapies across many tissue types. However, in practice many iPSC-derived cells have presented as immature in physiological function, and despite efforts to recapitulate adult maturity, most have yet to meet the necessary benchmarks for the intended tissues. Here, we summarize the available state of knowledge surrounding the physiological mechanisms underlying cell maturation in several key tissues. Common signaling consolidators, as well as potential synergies between critical signaling pathways are explored. Finally, current practices in physiologically relevant tissue engineering and experimental design are critically examined, with the goal of integrating greater decision paradigms and frameworks towards achieving efficient maturation strategies, which in turn may produce higher-valued iPSC-derived tissues. Nature Publishing Group UK 2022-09-03 /pmc/articles/PMC9440900/ /pubmed/36057642 http://dx.doi.org/10.1038/s41536-022-00246-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Perspective
Callaghan, Neal I.
Durland, Lauren J.
Ireland, Ronald G.
Santerre, J. Paul
Simmons, Craig A.
Davenport Huyer, Locke
Harnessing conserved signaling and metabolic pathways to enhance the maturation of functional engineered tissues
title Harnessing conserved signaling and metabolic pathways to enhance the maturation of functional engineered tissues
title_full Harnessing conserved signaling and metabolic pathways to enhance the maturation of functional engineered tissues
title_fullStr Harnessing conserved signaling and metabolic pathways to enhance the maturation of functional engineered tissues
title_full_unstemmed Harnessing conserved signaling and metabolic pathways to enhance the maturation of functional engineered tissues
title_short Harnessing conserved signaling and metabolic pathways to enhance the maturation of functional engineered tissues
title_sort harnessing conserved signaling and metabolic pathways to enhance the maturation of functional engineered tissues
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9440900/
https://www.ncbi.nlm.nih.gov/pubmed/36057642
http://dx.doi.org/10.1038/s41536-022-00246-3
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