Cardioids reveal self-organizing principles of human cardiogenesis

Organoids capable of forming tissue-like structures have transformed our ability to model human development and disease. With the notable exception of the human heart, lineage-specific self-organizing organoids have been reported for all major organs. Here, we established self-organizing cardioids from human pluripotent stem cells that intrinsically specify, pattern, and morph into chamber-like structures containing a cavity. Cardioid complexity can be controlled by signaling that instructs the separation of cardiomyocyte and endothelial layers and by directing epicardial spreading, inward migration, and differentiation. We find that cavity morphogenesis is governed by a mesodermal WNT-BMP signaling axis and requires its target HAND1, a transcription factor linked to developmental heart chamber defects. Upon cryoinjury, cardioids initiated a cell-type-dependent accumulation of extracellular matrix, an early hallmark of both regeneration and heart disease. Thus, human cardioids represent a powerful platform to mechanistically dissect self-organization, congenital heart defects and serve as a foundation for future translational research. [Display omitted] •Chamber-like cardioids form a cavity and recapitulate heart lineage architecture•Cardioid self-organization and lineage identity is instructed by signaling•WNT-BMP signaling directs cavity formation via HAND1•Cryoinjury initiates an in vivo-like fibronectin and collagen accumulation Cardioids that pattern and morph into chamber-like structures are established from human pluripotent stem cells.