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Kidney organoids: accurate models or fortunate accidents

There are now many reports of human kidney organoids generated via the directed differentiation of human pluripotent stem cells (PSCs) based on an existing understanding of mammalian kidney organogenesis. Such kidney organoids potentially represent tractable tools for the study of normal human devel...

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Detalles Bibliográficos
Autores principales: Little, Melissa H., Combes, Alexander N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771389/
https://www.ncbi.nlm.nih.gov/pubmed/31575677
http://dx.doi.org/10.1101/gad.329573.119
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author Little, Melissa H.
Combes, Alexander N.
author_facet Little, Melissa H.
Combes, Alexander N.
author_sort Little, Melissa H.
collection PubMed
description There are now many reports of human kidney organoids generated via the directed differentiation of human pluripotent stem cells (PSCs) based on an existing understanding of mammalian kidney organogenesis. Such kidney organoids potentially represent tractable tools for the study of normal human development and disease with improvements in scale, structure, and functional maturation potentially providing future options for renal regeneration. The utility of such organotypic models, however, will ultimately be determined by their developmental accuracy. While initially inferred from mouse models, recent transcriptional analyses of human fetal kidney have provided greater insight into nephrogenesis. In this review, we discuss how well human kidney organoids model the human fetal kidney and how the remaining differences challenge their utility.
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spelling pubmed-67713892020-04-01 Kidney organoids: accurate models or fortunate accidents Little, Melissa H. Combes, Alexander N. Genes Dev Review There are now many reports of human kidney organoids generated via the directed differentiation of human pluripotent stem cells (PSCs) based on an existing understanding of mammalian kidney organogenesis. Such kidney organoids potentially represent tractable tools for the study of normal human development and disease with improvements in scale, structure, and functional maturation potentially providing future options for renal regeneration. The utility of such organotypic models, however, will ultimately be determined by their developmental accuracy. While initially inferred from mouse models, recent transcriptional analyses of human fetal kidney have provided greater insight into nephrogenesis. In this review, we discuss how well human kidney organoids model the human fetal kidney and how the remaining differences challenge their utility. Cold Spring Harbor Laboratory Press 2019-10-01 /pmc/articles/PMC6771389/ /pubmed/31575677 http://dx.doi.org/10.1101/gad.329573.119 Text en © 2019 Little and Combes; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Review
Little, Melissa H.
Combes, Alexander N.
Kidney organoids: accurate models or fortunate accidents
title Kidney organoids: accurate models or fortunate accidents
title_full Kidney organoids: accurate models or fortunate accidents
title_fullStr Kidney organoids: accurate models or fortunate accidents
title_full_unstemmed Kidney organoids: accurate models or fortunate accidents
title_short Kidney organoids: accurate models or fortunate accidents
title_sort kidney organoids: accurate models or fortunate accidents
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771389/
https://www.ncbi.nlm.nih.gov/pubmed/31575677
http://dx.doi.org/10.1101/gad.329573.119
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