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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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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. |
format | Online Article Text |
id | pubmed-9440900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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