Key result
Stimulation of human cardiac organoids with 87 ligands established a perturbation atlas revealing functional clusters and an interferon-γ signaling signature driving HFpEF.
Why the study?
Large-scale perturbation atlases exist for systems biology, but no equivalent resource existed for the human heart measuring contractile function and transcriptomic state together.
The Cardiopedia-Ligand atlas provides a comprehensive resource linking ligand-receptor perturbations to functional and transcriptomic changes in human cardiac organoids, identifying novel pathways relevant to HFpEF.
Answers are grounded in this paper and cite their sources.
Offers a scalable resource for cardiac receptor pharmacology in organoids; leaves open in vivo validation and clinical translation.
Large-scale perturbation atlases have transformed systems biology, yet no equivalent resource exists for the human heart, where contractile function and transcriptomic state must be measured together. Here, we establish Cardiopedia-Ligand, a comprehensive perturbation-function-transcriptome atlas generated by stimulating human cardiac organoids (hCOs) with 87 ligands targeting 98 cell-membrane receptors expressed in the human heart. We developed an automated high-throughput pipeline enabling individualized contractility measurements and single-organoid mRNA sequencing. We use this pipeline to define both recognized and previously unrecognized functional and transcriptional clusters, including inotropes, endothelin peptides, extracellular matrix regulators, and multiple inflammatory clusters. Clustering analysis, machine learning, and the "fingerprinting" of human heart failure biopsies revealed previously underappreciated similarities between ligands and an interferon-γ signaling signature driving heart failure with preserved ejection fraction (HFpEF). Together, this comprehensive Cardiopedia-Ligand dataset provides a valuable and accessible resource for interrogating cardiac biology and human disease.
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Reid et al. (2026) studied Cardiac biology and human disease. 87 ligands targeting 98 cell-membrane receptors was evaluated on Contractility measurements and single-organoid mRNA sequencing. Stimulation of human cardiac organoids with 87 ligands established a perturbation atlas revealing functional clusters and an interferon-γ signaling signature driving HFpEF.
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