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Opportunities and Challenges of Human IPSC Technology in Kidney Disease Research

Human induced pluripotent stem cells (iPSCs), since their discovery in 2007, open a broad array of opportunities for research and potential therapeutic uses. The substantial progress in iPSC reprogramming, maintenance, differentiation, and characterization technologies since then has supported their...

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Detalles Bibliográficos
Autores principales: Lee, Jia-Jung, Lin, Chuang-Yu, Chen, Hung-Chun, Hsieh, Patrick C. H., Chiu, Yi-Wen, Chang, Jer-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9775669/
https://www.ncbi.nlm.nih.gov/pubmed/36551987
http://dx.doi.org/10.3390/biomedicines10123232
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author Lee, Jia-Jung
Lin, Chuang-Yu
Chen, Hung-Chun
Hsieh, Patrick C. H.
Chiu, Yi-Wen
Chang, Jer-Ming
author_facet Lee, Jia-Jung
Lin, Chuang-Yu
Chen, Hung-Chun
Hsieh, Patrick C. H.
Chiu, Yi-Wen
Chang, Jer-Ming
author_sort Lee, Jia-Jung
collection PubMed
description Human induced pluripotent stem cells (iPSCs), since their discovery in 2007, open a broad array of opportunities for research and potential therapeutic uses. The substantial progress in iPSC reprogramming, maintenance, differentiation, and characterization technologies since then has supported their applications from disease modeling and preclinical experimental platforms to the initiation of cell therapies. In this review, we started with a background introduction about stem cells and the discovery of iPSCs, examined the developing technologies in reprogramming and characterization, and provided the updated list of stem cell biobanks. We highlighted several important iPSC-based research including that on autosomal dominant kidney disease and SARS-CoV-2 kidney involvement and discussed challenges and future perspectives.
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spelling pubmed-97756692022-12-23 Opportunities and Challenges of Human IPSC Technology in Kidney Disease Research Lee, Jia-Jung Lin, Chuang-Yu Chen, Hung-Chun Hsieh, Patrick C. H. Chiu, Yi-Wen Chang, Jer-Ming Biomedicines Review Human induced pluripotent stem cells (iPSCs), since their discovery in 2007, open a broad array of opportunities for research and potential therapeutic uses. The substantial progress in iPSC reprogramming, maintenance, differentiation, and characterization technologies since then has supported their applications from disease modeling and preclinical experimental platforms to the initiation of cell therapies. In this review, we started with a background introduction about stem cells and the discovery of iPSCs, examined the developing technologies in reprogramming and characterization, and provided the updated list of stem cell biobanks. We highlighted several important iPSC-based research including that on autosomal dominant kidney disease and SARS-CoV-2 kidney involvement and discussed challenges and future perspectives. MDPI 2022-12-12 /pmc/articles/PMC9775669/ /pubmed/36551987 http://dx.doi.org/10.3390/biomedicines10123232 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Lee, Jia-Jung
Lin, Chuang-Yu
Chen, Hung-Chun
Hsieh, Patrick C. H.
Chiu, Yi-Wen
Chang, Jer-Ming
Opportunities and Challenges of Human IPSC Technology in Kidney Disease Research
title Opportunities and Challenges of Human IPSC Technology in Kidney Disease Research
title_full Opportunities and Challenges of Human IPSC Technology in Kidney Disease Research
title_fullStr Opportunities and Challenges of Human IPSC Technology in Kidney Disease Research
title_full_unstemmed Opportunities and Challenges of Human IPSC Technology in Kidney Disease Research
title_short Opportunities and Challenges of Human IPSC Technology in Kidney Disease Research
title_sort opportunities and challenges of human ipsc technology in kidney disease research
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9775669/
https://www.ncbi.nlm.nih.gov/pubmed/36551987
http://dx.doi.org/10.3390/biomedicines10123232
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