Vascular deficiencies in renal organoids and ex vivo kidney organogenesis.


Journal

Developmental biology
ISSN: 1095-564X
Titre abrégé: Dev Biol
Pays: United States
ID NLM: 0372762

Informations de publication

Date de publication:
09 2021
Historique:
received: 21 09 2020
revised: 24 04 2021
accepted: 27 04 2021
pubmed: 18 5 2021
medline: 14 10 2021
entrez: 17 5 2021
Statut: ppublish

Résumé

Chronic kidney disease (CKD) and end stage renal disease (ESRD) are increasingly frequent and devastating conditions that have driven a surge in the need for kidney transplantation. A stark shortage of organs has fueled interest in generating viable replacement tissues ex vivo for transplantation. One promising approach has been self-organizing organoids, which mimic developmental processes and yield multicellular, organ-specific tissues. However, a recognized roadblock to this approach is that many organoid cell types fail to acquire full maturity and function. Here, we comprehensively assess the vasculature in two distinct kidney organoid models as well as in explanted embryonic kidneys. Using a variety of methods, we show that while organoids can develop a wide range of kidney cell types, as previously shown, endothelial cells (ECs) initially arise but then rapidly regress over time in culture. Vasculature of cultured embryonic kidneys exhibit similar regression. By contrast, engraftment of kidney organoids under the kidney capsule results in the formation of a stable, perfused vasculature that integrates into the organoid. This work demonstrates that kidney organoids offer a promising model system to define the complexities of vascular-nephron interactions, but the establishment and maintenance of a vascular network present unique challenges when grown ex vivo.

Identifiants

pubmed: 34000274
pii: S0012-1606(21)00110-X
doi: 10.1016/j.ydbio.2021.04.009
pmc: PMC8382085
mid: NIHMS1728383
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

98-116

Subventions

Organisme : NIDDK NIH HHS
ID : F31 DK124046
Pays : United States

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

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Auteurs

Anne R Ryan (AR)

Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Alicia R England (AR)

Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Christopher P Chaney (CP)

Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Mitzy A Cowdin (MA)

Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Max Hiltabidle (M)

Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Edward Daniel (E)

Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Ashwani Kumar Gupta (AK)

University of Arizona, Tucson, AZ, USA.

Leif Oxburgh (L)

Rogosin Institute, NY, NY, USA.

Thomas J Carroll (TJ)

Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA; Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Ondine Cleaver (O)

Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA. Electronic address: ondine.cleaver@utsouthwestern.edu.

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Classifications MeSH