Modeling cardiac fibroblast heterogeneity from human pluripotent stem cell-derived epicardial cells

Ian Fernandes, Shunsuke Funakoshi (), Homaira Hamidzada, Slava Epelman and Gordon Keller ()
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Ian Fernandes: University Health Network
Shunsuke Funakoshi: University Health Network
Homaira Hamidzada: University Health Network Toronto
Slava Epelman: University Health Network Toronto
Gordon Keller: University Health Network

Nature Communications, 2023, vol. 14, issue 1, 1-19

Abstract: Abstract Cardiac fibroblasts play an essential role in the development of the heart and are implicated in disease progression in the context of fibrosis and regeneration. Here, we establish a simple organoid culture platform using human pluripotent stem cell-derived epicardial cells and ventricular cardiomyocytes to study the development, maturation, and heterogeneity of cardiac fibroblasts under normal conditions and following treatment with pathological stimuli. We demonstrate that this system models the early interactions between epicardial cells and cardiomyocytes to generate a population of fibroblasts that recapitulates many aspects of fibroblast behavior in vivo, including changes associated with maturation and in response to pathological stimuli associated with cardiac injury. Using single cell transcriptomics, we show that the hPSC-derived organoid fibroblast population displays a high degree of heterogeneity that approximates the heterogeneity of populations in both the normal and diseased human heart. Additionally, we identify a unique subpopulation of fibroblasts possessing reparative features previously characterized in the hearts of model organisms. Taken together, our system recapitulates many aspects of human cardiac fibroblast specification, development, and maturation, providing a platform to investigate the role of these cells in human cardiovascular development and disease.

Date: 2023
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43312-0

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DOI: 10.1038/s41467-023-43312-0

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