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Updated: Feb 23, 2026

A Simplified Method for Generating Kidney Organoids from Human Pluripotent Stem Cells
Published on: April 13, 2021
Concise Review: Kidney Generation with Human Pluripotent Stem Cells
Ryuji Morizane1,2,3, Tomoya Miyoshi1,2, Joseph V Bonventre1,2,3
1Department of Medicine, Renal Division, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Insights
Human pluripotent stem cells (hPSCs) offer a promising avenue for regenerating kidneys by generating nephron progenitor cells (NPCs). This research explores hPSC-derived NPCs for kidney disease modeling and regenerative therapies.
Area of Science:
- Regenerative Medicine
- Stem Cell Biology
- Nephrology
Background:
- Chronic kidney disease (CKD) is a global health issue causing significant mortality.
- Loss of nephrons in adult kidneys cannot be reversed, necessitating novel therapeutic strategies.
- Human pluripotent stem cells (hPSCs) possess the potential for kidney regenerative therapies.
Purpose of the Study:
- To review advancements in generating nephron progenitor cells (NPCs) and kidney cells from hPSCs.
- To discuss NPC expansion from embryonic kidneys and in vivo regeneration approaches.
- To highlight the potential of hPSC-derived cells for kidney disease modeling and drug screening.
Main Methods:
- Summarizing recent studies on inducing NPCs and kidney cells from hPSCs.
- Reviewing studies on NPC expansion from mouse and human embryonic kidneys.
- Discussing in vivo cell therapies and bioengineered kidney development.
Main Results:
- Protocols have been established to generate NPCs and nephron epithelial cells from hPSCs.
- Key signals for maintaining stemness of human NPCs in vitro have been identified.
- Large-scale production of human NPCs and kidney organoids is becoming feasible.
Conclusions:
- hPSC-derived NPCs are crucial for advancing kidney regenerative medicine.
- These cells hold promise for understanding kidney development, disease modeling, and therapeutic interventions.
- Future research focuses on in vivo regeneration and bioengineered kidney development.
Abstract:
Chronic kidney disease (CKD) is a worldwide health care problem, resulting in increased cardiovascular mortality and often leading to end-stage kidney disease, where patients require kidney replacement therapies such as hemodialysis or kidney transplantation. Loss of functional nephrons contributes to the progression of CKD, which can be attenuated but not reversed due to inability to generate new nephrons in human adult kidneys. Human pluripotent stem cells (hPSCs), by virtue of their unlimited self-renewal and ability to differentiate into cells of all three embryonic germ layers, are attractive sources for kidney regenerative therapies. Recent advances in stem cell biology have identified key signals necessary to maintain stemness of human nephron progenitor cells (NPCs) in vitro, and led to establishment of protocols to generate NPCs and nephron epithelial cells from human fetal kidneys and hPSCs. Effective production of large amounts of human NPCs and kidney organoids will facilitate elucidation of developmental and pathobiological pathways, kidney disease modeling and drug screening as well as kidney regenerative therapies. We summarize the recent studies to induce NPCs and kidney cells from hPSCs, studies of NPC expansion from mouse and human embryonic kidneys, and discuss possible approaches in vivo to regenerate kidneys with cell therapies and the development of bioengineered kidneys. Stem Cells 2017;35:2209-2217.
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