Spatially organized cellular communities form the developing human heart

• 成果类型: Article
• 署名作者: Farah, Elie N.; Hu, Robert K.; Kern, Colin; Zhang, Qingquan; Lu, Ting-Yu; Ma, Qixuan; Tran, Shaina; Zhang, Bo; Carlin, Daniel; Monell, Alexander; Blair, Andrew P.; Wang, Zilu; Eschbach, Jacqueline; Li, Bin; Destici, Eugin; Ren, Bing; Evans, Sylvia M.; Chen, Shaochen; Zhu, Quan; Chi, Neil C.
• 署名单位: University of California System; University of California San Diego; University of California System; University of California San Diego; University of California System; University of California San Diego; University of California System; University of California San Diego; University of California System; University of California San Diego; Ludwig Institute for Cancer Research; University of California System; University of California San Diego; University of California System; University of California San Diego; University of California System; University of California San Diego; University of California System; University of California San Diego
• 刊物名称: Nature
• ISSN/ISSBN: 0028-4972
• DOI: 10.1038/s41586-024-07171-z
• 发表日期: 2024-03-28
• 页码: 854-+
• 关键词: transcriptomic data; gene-expression; lineage; cells; differentiation; proliferation; environment; DESIGN; origin; GROWTH

摘要

The heart, which is the first organ to develop, is highly dependent on its form to function(1,2). However, how diverse cardiac cell types spatially coordinate to create the complex morphological structures that are crucial for heart function remains unclear. Here we integrated single-cell RNA-sequencing with high-resolution multiplexed error-robust fluorescence in situ hybridization to resolve the identity of the cardiac cell types that develop the human heart. This approach also provided a spatial mapping of individual cells that enables illumination of their organization into cellular communities that form distinct cardiac structures. We discovered that many of these cardiac cell types further specified into subpopulations exclusive to specific communities, which support their specialization according to the cellular ecosystem and anatomical region. In particular, ventricular cardiomyocyte subpopulations displayed an unexpected complex laminar organization across the ventricular wall and formed, with other cell subpopulations, several cellular communities. Interrogating cell-cell interactions within these communities using in vivo conditional genetic mouse models and in vitro human pluripotent stem cell systems revealed multicellular signalling pathways that orchestrate the spatial organization of cardiac cell subpopulations during ventricular wall morphogenesis. These detailed findings into the cellular social interactions and specialization of cardiac cell types constructing and remodelling the human heart offer new insights into structural heart diseases and the engineering of complex multicellular tissues for human heart repair.