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 HukriedePublished 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.