Molecular Medicine Laboratory, International Centre for Genetic Engineering and Biotechnology (ICGEB), Trieste, Italy.
Fondazione Cardiocentro Ticino and Swiss Institute for Regenerative Medicine, Lugano, Switzerland.
J Cell Mol Med. 2018 Nov;22(11):5583-5595. doi: 10.1111/jcmm.13832. Epub 2018 Aug 23.
Cardiospheres (CSps) are self-assembling clusters of a heterogeneous population of poorly differentiated cells outgrowing from in vitro cultured cardiac explants. Scanty information is available on the molecular pathways regulating CSp growth and their differentiation potential towards cardiac and vascular lineages. Here we report that Notch1 stimulates a massive increase in both CSp number and size, inducing a peculiar gene expression programme leading to a cardiovascular molecular signature. These effects were further enhanced using Adeno-Associated Virus (AAV)-based gene transfer of activated Notch1-intracellular domain (N1-ICD) or soluble-Jagged1 (sJ1) ligand to CSp-forming cells. A peculiar effect was exploited by selected pro-proliferating miRNAs: hsa-miR-590-3p induced a cardiovascular gene expression programme, while hsa-miR-199a-3p acted as the most potent stimulus for the activation of the Notch pathway, thus showing that, unlike in adult cardiomyocytes, these miRNAs involve Notch signalling activation in CSps. Our results identify Notch1 as a crucial regulator of CSp growth and differentiation along the vascular lineage, raising the attracting possibility that forced activation of this pathway might be exploited to promote in vitro CSp expansion as a tool for toxicology screening and cell-free therapeutic strategies.
心肌细胞球体(CSps)是从体外培养的心脏外植体中生长出的异质细胞的自组装簇。关于调节 CSp 生长及其向心脏和血管谱系分化的潜力的分子途径的信息很少。在这里,我们报告 Notch1 刺激 CSp 数量和大小的大量增加,诱导导致心血管分子特征的特殊基因表达程序。通过使用腺相关病毒(AAV)为基础的激活 Notch1 细胞内结构域(N1-ICD)或可溶性 Jagged1(sJ1)配体的基因转移到 CSp 形成细胞,进一步增强了这些效果。一些具有特殊促增殖作用的 miRNA 发挥了独特的作用:hsa-miR-590-3p 诱导心血管基因表达程序,而 hsa-miR-199a-3p 作为 Notch 途径激活的最强刺激物,从而表明与成年心肌细胞不同,这些 miRNA 涉及 CSp 中的 Notch 信号激活。我们的研究结果确定 Notch1 是 CSp 生长和沿血管谱系分化的关键调节剂,提出了一个有吸引力的可能性,即强制激活该途径可能被用来促进体外 CSp 的扩增,作为毒理学筛选和无细胞治疗策略的工具。