| Literature DB >> 33176168 |
Giuliana Rossi1, Nicolas Broguiere1, Matthew Miyamoto2, Andrea Boni3, Romain Guiet4, Mehmet Girgin1, Robert G Kelly5, Chulan Kwon2, Matthias P Lutolf6.
Abstract
Organoids are powerful models for studying tissue development, physiology, and disease. However, current culture systems disrupt the inductive tissue-tissue interactions needed for the complex morphogenetic processes of native organogenesis. Here, we show that mouse embryonic stem cells (mESCs) can be coaxed to robustly undergo fundamental steps of early heart organogenesis with an in-vivo-like spatiotemporal fidelity. These axially patterned embryonic organoids (gastruloids) mimic embryonic development and support the generation of cardiovascular progenitors, including first and second heart fields. The cardiac progenitors self-organize into an anterior domain reminiscent of a cardiac crescent before forming a beating cardiac tissue near a putative primitive gut-like tube, from which it is separated by an endocardial-like layer. These findings unveil the surprising morphogenetic potential of mESCs to execute key aspects of organogenesis through the coordinated development of multiple tissues. This platform could be an excellent tool for studying heart development in unprecedented detail and throughput.Entities:
Keywords: 3D cardiac tissue; cardiac organoid; cardiogenesis; development; embryonic organoids; heart; in vitro organogenesis
Mesh:
Year: 2020 PMID: 33176168 PMCID: PMC7867643 DOI: 10.1016/j.stem.2020.10.013
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633