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Cellular plasticity and diversity during heart valve epithelial-to-mesenchymal transitions revealed using single-cell RNA-seq

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We have generated scRNA-seq data from embryonic day (E)10.5 and E12.5 atrioventricular canals (primitive heart valves) to assess cellular diversity during the distinct epithelial-to-mesenchymal transitions (EMTs) from endocardium and epicardium that guide the formation of valve mesenchyme. Alongside, wildtype atrioventricular canals, we generated scRNA-seq data from Sox9 conditional knockouts (Sox9fl/fl;Tie2-cre) to explore the role of SOX9 in EMT. Atrioventricular canals were microdissected from cardiac chambers and outflow tract, enriching for heart valve progenitor lineages.

本研究生成了胚胎日(E)10.5与E12.5房室管(原始心瓣膜)的单细胞RNA测序(single-cell RNA sequencing, scRNA-seq)数据,用于评估引导瓣膜间充质形成的、源自心内膜与心外膜的不同上皮间质转化(epithelial-to-mesenchymal transitions, EMTs)过程中的细胞多样性。除野生型房室管样本外,我们还从Sox9条件性敲除小鼠(Sox9fl/fl;Tie2-cre)中获取了scRNA-seq数据,以探究SOX9在上皮间质转化中的作用。本研究中的房室管均从心腔与流出道中显微解剖获得,以富集心瓣膜祖细胞谱系。

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