Recent advances in renal regeneration

F1000Res. 2019 Feb 25:8:F1000 Faculty Rev-216. doi: 10.12688/f1000research.17127.1. eCollection 2019.

Abstract

Regeneration of a functional kidney from pluripotent stem cells (PSCs) is challenging because of its complex structure. Kidneys are derived from embryonic metanephros, which are composed of three progenitor cells: nephron progenitors, ureteric bud, and stromal progenitors. Nephron progenitors and ureteric bud have been induced successfully from PSCs as a result of the understanding of their detailed developmental process through cell-lineage tracing analysis. Moreover, these induced progenitors can be used to reconstruct the three-dimensional (3D) structure of kidneys in vitro, including glomeruli with podocytes, renal tubules, and the branching ureters. Induction of the remaining renal progenitors (that is, stromal progenitors from PSCs and the further maturation of reconstructed kidneys) needs to be studied extensively to regenerate functional and sophisticated kidneys from PSCs. In addition to the proper induction of renal progenitors, new bioengineering methods such as decellularization and 3D bioprinting and the recent advancements in the regeneration of kidneys in other species are promising leads for regenerating the complex spatial arrangement of kidneys, including the vascular network and urinary excretion pathway in humans.

Keywords: kidney; pluripotent stem cells; renegeration.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Cell Differentiation
  • Humans
  • Kidney / growth & development*
  • Nephrons / cytology*
  • Regeneration*
  • Stem Cells / cytology*
  • Tissue Engineering*

Grants and funding

This work was supported by Grant-in-Aid for Scientific Research (B) (JSPS KAKENHI grant 18H02824 to MN), Grant-in-Aid for Scientific Research (C) (JSPS KAKENHI grant 17K09688 to TT), and Grants-in-Aid for Scientific Research on Innovative Areas (KAKENHI grants 26111003 to MN).