Disease Modeling with Kidney Organoids

Kidney diseases often lack optimal treatments, causing millions of deaths each year. Thus, developing appropriate model systems to study human kidney disease is of utmost importance. Some of the most promising human kidney models are organoids or small organ-resembling tissue collectives, derived fr...

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Main Authors: Sophie Karp, Martin R Pollak, Balajikarthick Subramanian
Format: Article
Language:English
Published: MDPI AG 2022-08-01
Series:Micromachines
Subjects:
Online Access:https://www.mdpi.com/2072-666X/13/9/1384
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author Sophie Karp
Martin R Pollak
Balajikarthick Subramanian
author_facet Sophie Karp
Martin R Pollak
Balajikarthick Subramanian
author_sort Sophie Karp
collection DOAJ
description Kidney diseases often lack optimal treatments, causing millions of deaths each year. Thus, developing appropriate model systems to study human kidney disease is of utmost importance. Some of the most promising human kidney models are organoids or small organ-resembling tissue collectives, derived from human-induced pluripotent stem cells (hiPSCs). However, they are more akin to a first-trimester fetal kidney than an adult kidney. Therefore, new strategies are needed to advance their maturity. They have great potential for disease modeling and eventually auxiliary therapy if they can reach the maturity of an adult kidney. In this review, we will discuss the current state of kidney organoids in terms of their similarity to the human kidney and use as a disease modeling system thus far. We will then discuss potential pathways to advance the maturity of kidney organoids to match an adult kidney for more accurate human disease modeling.
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spelling doaj.art-e2652e6f25b948f6a58a8927dd2775532023-11-23T17:48:37ZengMDPI AGMicromachines2072-666X2022-08-01139138410.3390/mi13091384Disease Modeling with Kidney OrganoidsSophie Karp0Martin R Pollak1Balajikarthick Subramanian2Division of Nephrology, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USADivision of Nephrology, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USADivision of Nephrology, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USAKidney diseases often lack optimal treatments, causing millions of deaths each year. Thus, developing appropriate model systems to study human kidney disease is of utmost importance. Some of the most promising human kidney models are organoids or small organ-resembling tissue collectives, derived from human-induced pluripotent stem cells (hiPSCs). However, they are more akin to a first-trimester fetal kidney than an adult kidney. Therefore, new strategies are needed to advance their maturity. They have great potential for disease modeling and eventually auxiliary therapy if they can reach the maturity of an adult kidney. In this review, we will discuss the current state of kidney organoids in terms of their similarity to the human kidney and use as a disease modeling system thus far. We will then discuss potential pathways to advance the maturity of kidney organoids to match an adult kidney for more accurate human disease modeling.https://www.mdpi.com/2072-666X/13/9/1384organoidskidneydevelopmentmetanephrosureterictubule
spellingShingle Sophie Karp
Martin R Pollak
Balajikarthick Subramanian
Disease Modeling with Kidney Organoids
Micromachines
organoids
kidney
development
metanephros
ureteric
tubule
title Disease Modeling with Kidney Organoids
title_full Disease Modeling with Kidney Organoids
title_fullStr Disease Modeling with Kidney Organoids
title_full_unstemmed Disease Modeling with Kidney Organoids
title_short Disease Modeling with Kidney Organoids
title_sort disease modeling with kidney organoids
topic organoids
kidney
development
metanephros
ureteric
tubule
url https://www.mdpi.com/2072-666X/13/9/1384
work_keys_str_mv AT sophiekarp diseasemodelingwithkidneyorganoids
AT martinrpollak diseasemodelingwithkidneyorganoids
AT balajikarthicksubramanian diseasemodelingwithkidneyorganoids