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Updated: Jan 21, 2026

A Simplified Method for Generating Kidney Organoids from Human Pluripotent Stem Cells
Published on: April 13, 2021
Human kidney organoids: progress and remaining challenges
1Institute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto, Japan. ryuichi@kumamoto-u.ac.jp.
Abstract:
Kidney organoids are regarded as important tools with which to study the development of the normal and diseased human kidney. Since the first reports of human pluripotent stem cell-derived kidney organoids 5 years ago, kidney organoids have been successfully used to model glomerular and tubular diseases. In parallel, advances in single-cell RNA sequencing have led to identification of a variety of cell types in the organoids, and have shown these to be similar to, but more immature than, human kidney cells in vivo. Protocols for the in vitro expansion of stem cell-derived nephron progenitor cells (NPCs), as well as those for the selective induction of specific lineages, especially glomerular podocytes, have also been reported. Although most current organoids are based on the induction of NPCs, an induction protocol for ureteric buds (collecting duct precursors) has also been developed, and approaches to generate more complex kidney structures may soon be possible. Maturation of organoids is a major challenge, and more detailed analysis of the developing kidney at a single cell level is needed. Eventually, organotypic kidney structures equipped with nephrons, collecting ducts, ureters, stroma and vascular flow are required to generate transplantable kidneys; such attempts are in progress.
Insights
Kidney organoids derived from human pluripotent stem cells model kidney diseases. Further research is needed to mature these organoids for potential transplantation.
Area of Science:
- Developmental Biology
- Regenerative Medicine
- Stem Cell Biology
Background:
- Kidney organoids are valuable tools for studying human kidney development and disease.
- Recent advances include modeling glomerular and tubular diseases and identifying cell types via single-cell RNA sequencing.
- Organoids currently exhibit immature cell types compared to in vivo human kidney cells.
Purpose of the Study:
- To review the progress and challenges in developing kidney organoids.
- To highlight advancements in cell type induction and organoid complexity.
- To discuss the future directions for generating more mature and functional kidney structures.
Main Methods:
- Utilizing human pluripotent stem cells to generate kidney organoids.
- Employing single-cell RNA sequencing for cell type identification and characterization.
- Developing protocols for in vitro expansion and lineage-specific induction of kidney cells.
Main Results:
- Kidney organoids successfully model various kidney diseases.
- Single-cell RNA sequencing reveals cell types similar but immature to in vivo counterparts.
- Protocols for inducing nephron progenitor cells (NPCs) and ureteric buds have been established.
Conclusions:
- Kidney organoid technology has advanced significantly for disease modeling.
- Maturation and achieving in vivo-like complexity remain key challenges.
- Generating transplantable, organotypic kidney structures is an ongoing goal.
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