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Genetically engineering endothelial niche in human kidney organoids enables multilineage maturation, vascularization and de novo cell types.

Joseph C MaggioreRyan LeGrawAneta J PrzepiorskiJeremy VelazquezChristopher ChaneyEvan StreeterAnne C S BarbosaJonathan M FranksJoshua HislopAlex HillHaojia WuKatherine E PfisterSara E HowdenSimon C WatkinsMelissa H LittleBenjamin D HumphreysAlan M WatsonDonna Beer StolzSamira KianiAlan J DavidsonThomas J CarrollOndine CleaverSunder Sims-LucasMo R EbrahimkhaniNeil A Hukriede
Published in: bioRxiv : the preprint server for biology (2023)
model. Human kidney organoids are an attractive model to recapitulate kidney physiology, however, they are limited by the absence of a vascular network and mature cell populations. In this work, we have generated a genetically inducible endothelial niche that, when combined with an established kidney organoid protocol, induces the maturation of a robust endothelial cell network, induces a more mature podocyte population, and induces the emergence a functional renin population. This advance significantly increases the clinical relevance of human kidney organoids for etiological studies of kidney disease and future regenerative medicine strategies.
Keyphrases
  • endothelial cells
  • induced pluripotent stem cells
  • high glucose
  • randomized controlled trial
  • single cell
  • cell therapy
  • stem cells
  • bone marrow
  • mesenchymal stem cells