Micropatterned Organoids Enable Modeling of the Earliest Stages of Human Cardiac Vascularization
Oscar John AbileziD, Huaxiao YangiD, Yuan GuaniD, Mengcheng SheniD, Zehra YıldırımiD, Yan ZhugeiD, Ravichandra VenkateshappaiD, Shane Rui ZhaoiD, Angello Huerta Gomez, Marcel El‐Mokahal, Logan Dunkenberger, Yoshikazu OnoiD, Masafumi ShibataiD, Peter N. NwokoyeiD, Lei TianiD, Kitchener D. WilsoniD, Evan H. LyalliD, Fangjun JiaiD, Hung-Ta WoiD, Gao ZhouiD, Bryan AldanaiD, Ioannis KarakikesiD, Detlef ObaliD, Gary PeltziD, Christopher Kristaps ZarinsiD, Joseph C. WuiD
Abstract
Although model organisms have provided insight into the earliest stages of cardiac vascularization, we know very little about this process in humans. Here we show that spatially micropatterned human pluripotent stem cells (hPSCs) enable in vitro modeling of this process, corresponding to the first three weeks of in vivo human development. Using four hPSC fluorescent reporter lines, we create cardiac vascular organoids (cVOs) by identifying conditions that simultaneously give rise to spatially organized and branched vascular networks within endocardial, myocardial, and epicardial cells. Using single-cell transcriptomics, we show that the cellular composition of cVOs resembles that of a 6.5 post-conception week (PCW) human heart. We find that NOTCH and BMP pathways are upregulated in cVOs, and their inhibition disrupts vascularization. Finally, using the same vascular-inducing factors to create cVOs, we produce hepatic vascular organoids (hVOs). This suggests there is a conserved developmental program for creating vasculature within different organ systems. Graphic Abstract O_FIG O_LINKSMALLFIG WIDTH=159 HEIGHT=200 SRC="FIGDIR/small/499233v1_ufig1.gif" ALT="Figure 1"> View larger version (32K): org.highwire.dtl.DTLVardef@17b265org.highwire.dtl.DTLVardef@1c1113eorg.highwire.dtl.DTLVardef@531c18org.highwire.dtl.DTLVardef@596bd2_HPS_FORMAT_FIGEXP M_FIG C_FIG
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