Development and intra-renal delivery of renal progenitor organoids for effective integration in vivo

Renal progenitor organoids have been proposed as a source of tissue for kidney regeneration; however, their clinical translatability has not been demonstrated due to an inability to mass-produce comprehensive renal progenitor organoids and the lack of an effective intra-renal delivery platform that facilitates rapid integration into functionally meaningful sites. This study addresses these shortcomings. Human-induced pluripotent stem cells were differentiated into renal progenitor cells using an established protocol and aggregated using a novel assembly method to produce high yields of organoids. Organoids were encapsulated in collagen-based scaffolds for in vitro study and in vivo implantation into mouse renal cortex. In vitro, the organoids demonstrated sustained cell viability and renal structure maturation over time. In vivo delivered organoids showed rapid integration into host renal parenchyma while showing tubular and glomerular-like structure development and maturity markers. This proof-of-concept study presents many promising results, providing a system of renal organoid formation and delivery that may support the development of clinically translatable therapies and the advancement of in vitro renal organoid studies.

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Publication Details

Journal
Stem Cells Translational Medicine
Published
2024-10-28
DOI
https://doi.org/10.1093/stcltm/szae078
Citations
4
Primary Topic
Renal and related cancers
Type
article
Field-Weighted Citation Impact
0.94

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Development and intra-renal delivery of renal progenitor organoids for effective integration in vivo

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Renal and related cancers
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article

Development and intra-renal delivery of renal progenitor organoids for effective integration in vivo

Anthony Atala, Ickhee Kim, Diana Lim, Jihyun Kim, James J. Yoo, Qianqian Song, John David Jackson
article en
4 citations

Abstract

Renal progenitor organoids have been proposed as a source of tissue for kidney regeneration; however, their clinical translatability has not been demonstrated due to an inability to mass-produce comprehensive renal progenitor organoids and the lack of an effective intra-renal delivery platform that facilitates rapid integration into functionally meaningful sites. This study addresses these shortcomings. Human-induced pluripotent stem cells were differentiated into renal progenitor cells using an established protocol and aggregated using a novel assembly method to produce high yields of organoids. Organoids were encapsulated in collagen-based scaffolds for in vitro study and in vivo implantation into mouse renal cortex. In vitro, the organoids demonstrated sustained cell viability and renal structure maturation over time. In vivo delivered organoids showed rapid integration into host renal parenchyma while showing tubular and glomerular-like structure development and maturity markers. This proof-of-concept study presents many promising results, providing a system of renal organoid formation and delivery that may support the development of clinically translatable therapies and the advancement of in vitro renal organoid studies.

Stem Cells Translational MedicineVol. 14(1)
Forest Institute (US), Wake Forest University (US)
National Institutes of Health
Openalex Percentile: Top 25%
Renal and related cancers
0.94
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