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Translating Organoids into Artificial Kidneys

PURPOSE OF REVIEW: Kidney disease affects more than 13% of the world population, and current treatment options are limited to dialysis and organ transplantation. The generation of kidney organoids from human-induced pluripotent stem (hiPS) cells could be harnessed to engineer artificial organs and h...

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Autores principales: Kalejaiye, Titilola D., Barreto, Amanda D., Musah, Samira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9592871/
https://www.ncbi.nlm.nih.gov/pubmed/36311696
http://dx.doi.org/10.1007/s40472-022-00383-0
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author Kalejaiye, Titilola D.
Barreto, Amanda D.
Musah, Samira
author_facet Kalejaiye, Titilola D.
Barreto, Amanda D.
Musah, Samira
author_sort Kalejaiye, Titilola D.
collection PubMed
description PURPOSE OF REVIEW: Kidney disease affects more than 13% of the world population, and current treatment options are limited to dialysis and organ transplantation. The generation of kidney organoids from human-induced pluripotent stem (hiPS) cells could be harnessed to engineer artificial organs and help overcome the challenges associated with the limited supply of transplantable kidneys. The purpose of this article is to review the progress in kidney organoid generation and transplantation and highlight some existing challenges in the field. We also examined possible improvements that could help realize the potential of organoids as artificial organs or alternatives for kidney transplantation therapy. RECENT FINDINGS: Organoids are useful for understanding the mechanisms of kidney development, and they provide robust platforms for drug screening, disease modeling, and generation of tissues for organ replacement therapies. Efforts to design organoids rely on the ability of cells to self-assemble and pattern themselves into recognizable tissues. While existing protocols for generating organoids result in multicellular structures reminiscent of the developing kidney, many do not yet fully recapitulate the complex cellular composition, structure, and functions of the intact kidney. Recent advances toward achieving these goals include identifying cell culture conditions that produce organoids with improved vasculature and cell maturation and functional states. Still, additional improvements are needed to enhance tissue patterning, specialization, and function, and avoid tumorigenicity after transplantation. SUMMARY: This report focuses on kidney organoid studies, advancements and limitations, and future directions for improvements towards transplantation.
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spelling pubmed-95928712022-10-25 Translating Organoids into Artificial Kidneys Kalejaiye, Titilola D. Barreto, Amanda D. Musah, Samira Curr Transplant Rep Cellular Transplants (A Asthana and G Orlando, Section Editors) PURPOSE OF REVIEW: Kidney disease affects more than 13% of the world population, and current treatment options are limited to dialysis and organ transplantation. The generation of kidney organoids from human-induced pluripotent stem (hiPS) cells could be harnessed to engineer artificial organs and help overcome the challenges associated with the limited supply of transplantable kidneys. The purpose of this article is to review the progress in kidney organoid generation and transplantation and highlight some existing challenges in the field. We also examined possible improvements that could help realize the potential of organoids as artificial organs or alternatives for kidney transplantation therapy. RECENT FINDINGS: Organoids are useful for understanding the mechanisms of kidney development, and they provide robust platforms for drug screening, disease modeling, and generation of tissues for organ replacement therapies. Efforts to design organoids rely on the ability of cells to self-assemble and pattern themselves into recognizable tissues. While existing protocols for generating organoids result in multicellular structures reminiscent of the developing kidney, many do not yet fully recapitulate the complex cellular composition, structure, and functions of the intact kidney. Recent advances toward achieving these goals include identifying cell culture conditions that produce organoids with improved vasculature and cell maturation and functional states. Still, additional improvements are needed to enhance tissue patterning, specialization, and function, and avoid tumorigenicity after transplantation. SUMMARY: This report focuses on kidney organoid studies, advancements and limitations, and future directions for improvements towards transplantation. Springer International Publishing 2022-10-25 2022 /pmc/articles/PMC9592871/ /pubmed/36311696 http://dx.doi.org/10.1007/s40472-022-00383-0 Text en © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2022, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Cellular Transplants (A Asthana and G Orlando, Section Editors)
Kalejaiye, Titilola D.
Barreto, Amanda D.
Musah, Samira
Translating Organoids into Artificial Kidneys
title Translating Organoids into Artificial Kidneys
title_full Translating Organoids into Artificial Kidneys
title_fullStr Translating Organoids into Artificial Kidneys
title_full_unstemmed Translating Organoids into Artificial Kidneys
title_short Translating Organoids into Artificial Kidneys
title_sort translating organoids into artificial kidneys
topic Cellular Transplants (A Asthana and G Orlando, Section Editors)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9592871/
https://www.ncbi.nlm.nih.gov/pubmed/36311696
http://dx.doi.org/10.1007/s40472-022-00383-0
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