4.4 Review

Kidney organoids in translational medicine: Disease modeling and regenerative medicine

Journal

DEVELOPMENTAL DYNAMICS
Volume 249, Issue 1, Pages 34-45

Publisher

WILEY
DOI: 10.1002/dvdy.22

Keywords

disease modeling; kidney; nephron; organoid; pluripotent stem cell; regeneration

Funding

  1. NCATS NIH HHS [UH3 TR002155, UG3 TR002155] Funding Source: Medline
  2. NHGRI NIH HHS [UM1 HG009390] Funding Source: Medline
  3. NIBIB NIH HHS [U01 EB028899] Funding Source: Medline
  4. NIDDK NIH HHS [U01 DK127587, DP2 DK133821, UC2 DK126023, U24 DK076169] Funding Source: Medline

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The kidney is one of the most complex organs composed of multiple cell types, functioning to maintain homeostasis by means of the filtering of metabolic wastes, balancing of blood electrolytes, and adjustment of blood pressure. Recent advances in 3D culture technologies in vitro enabled the generation of organoids which mimic the structure and function of in vivo organs. Organoid technology has allowed for new insights into human organ development and human pathophysiology, with great potential for translational research. Increasing evidence shows that kidney organoids are a useful platform for disease modeling of genetic kidney diseases when derived from genetic patient iPSCs and/or CRISPR-mutated stem cells. Although single cell RNA-seq studies highlight the technical difficulties underlying kidney organoid generation reproducibility and variation in differentiation protocols, kidney organoids still hold great potential to understand kidney pathophysiology as applied to kidney injury and fibrosis. In this review, we summarize various studies of kidney organoids, disease modeling, genome-editing, and bioengineering, and additionally discuss the potential of and current challenges to kidney organoid research.

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