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Tubuloid culture enables long-term expansion of functional human kidney tubule epithelium from iPSC-derived organoids

Kidney organoids generated from induced pluripotent stem cells (iPSC) have proven valuable for studies of kidney development, disease, and therapeutic screening. However, specific applications have been hampered by limited expansion capacity, immaturity, off-target cells, and inability to access the...

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Autores principales: Yousef Yengej, Fjodor A., Jansen, Jitske, Ammerlaan, Carola M. E., Dilmen, Emre, Pou Casellas, Carla, Masereeuw, Rosalinde, Hoenderop, Joost G., Smeets, Bart, Rookmaaker, Maarten B., Verhaar, Marianne C., Clevers, Hans
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9963523/
https://www.ncbi.nlm.nih.gov/pubmed/36724260
http://dx.doi.org/10.1073/pnas.2216836120
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author Yousef Yengej, Fjodor A.
Jansen, Jitske
Ammerlaan, Carola M. E.
Dilmen, Emre
Pou Casellas, Carla
Masereeuw, Rosalinde
Hoenderop, Joost G.
Smeets, Bart
Rookmaaker, Maarten B.
Verhaar, Marianne C.
Clevers, Hans
author_facet Yousef Yengej, Fjodor A.
Jansen, Jitske
Ammerlaan, Carola M. E.
Dilmen, Emre
Pou Casellas, Carla
Masereeuw, Rosalinde
Hoenderop, Joost G.
Smeets, Bart
Rookmaaker, Maarten B.
Verhaar, Marianne C.
Clevers, Hans
author_sort Yousef Yengej, Fjodor A.
collection PubMed
description Kidney organoids generated from induced pluripotent stem cells (iPSC) have proven valuable for studies of kidney development, disease, and therapeutic screening. However, specific applications have been hampered by limited expansion capacity, immaturity, off-target cells, and inability to access the apical side. Here, we apply recently developed tubuloid protocols to purify and propagate kidney epithelium from d7+18 (post nephrogenesis) iPSC-derived organoids. The resulting ‘iPSC organoid-derived (iPSCod)’ tubuloids can be exponentially expanded for at least 2.5 mo, while retaining expression of important tubular transporters and segment-specific markers. This approach allows for selective propagation of the mature tubular epithelium, as immature cells, stroma, and undesirable off-target cells rapidly disappeared. iPSCod tubuloids provide easy apical access, which enabled functional evaluation and demonstration of essential secretion and electrolyte reabsorption processes. In conclusion, iPSCod tubuloids provide a different, complementary human kidney model that unlocks opportunities for functional characterization, disease modeling, and regenerative nephrology.
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spelling pubmed-99635232023-02-26 Tubuloid culture enables long-term expansion of functional human kidney tubule epithelium from iPSC-derived organoids Yousef Yengej, Fjodor A. Jansen, Jitske Ammerlaan, Carola M. E. Dilmen, Emre Pou Casellas, Carla Masereeuw, Rosalinde Hoenderop, Joost G. Smeets, Bart Rookmaaker, Maarten B. Verhaar, Marianne C. Clevers, Hans Proc Natl Acad Sci U S A Biological Sciences Kidney organoids generated from induced pluripotent stem cells (iPSC) have proven valuable for studies of kidney development, disease, and therapeutic screening. However, specific applications have been hampered by limited expansion capacity, immaturity, off-target cells, and inability to access the apical side. Here, we apply recently developed tubuloid protocols to purify and propagate kidney epithelium from d7+18 (post nephrogenesis) iPSC-derived organoids. The resulting ‘iPSC organoid-derived (iPSCod)’ tubuloids can be exponentially expanded for at least 2.5 mo, while retaining expression of important tubular transporters and segment-specific markers. This approach allows for selective propagation of the mature tubular epithelium, as immature cells, stroma, and undesirable off-target cells rapidly disappeared. iPSCod tubuloids provide easy apical access, which enabled functional evaluation and demonstration of essential secretion and electrolyte reabsorption processes. In conclusion, iPSCod tubuloids provide a different, complementary human kidney model that unlocks opportunities for functional characterization, disease modeling, and regenerative nephrology. National Academy of Sciences 2023-02-01 2023-02-07 /pmc/articles/PMC9963523/ /pubmed/36724260 http://dx.doi.org/10.1073/pnas.2216836120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Yousef Yengej, Fjodor A.
Jansen, Jitske
Ammerlaan, Carola M. E.
Dilmen, Emre
Pou Casellas, Carla
Masereeuw, Rosalinde
Hoenderop, Joost G.
Smeets, Bart
Rookmaaker, Maarten B.
Verhaar, Marianne C.
Clevers, Hans
Tubuloid culture enables long-term expansion of functional human kidney tubule epithelium from iPSC-derived organoids
title Tubuloid culture enables long-term expansion of functional human kidney tubule epithelium from iPSC-derived organoids
title_full Tubuloid culture enables long-term expansion of functional human kidney tubule epithelium from iPSC-derived organoids
title_fullStr Tubuloid culture enables long-term expansion of functional human kidney tubule epithelium from iPSC-derived organoids
title_full_unstemmed Tubuloid culture enables long-term expansion of functional human kidney tubule epithelium from iPSC-derived organoids
title_short Tubuloid culture enables long-term expansion of functional human kidney tubule epithelium from iPSC-derived organoids
title_sort tubuloid culture enables long-term expansion of functional human kidney tubule epithelium from ipsc-derived organoids
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9963523/
https://www.ncbi.nlm.nih.gov/pubmed/36724260
http://dx.doi.org/10.1073/pnas.2216836120
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