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Human induced pluripotent stem cell-derived vocal fold mucosa mimics development and responses to smoke exposure

机译:人类诱导的多能干细胞来源的声带粘膜模仿烟的形成和对烟尘的反应

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摘要

Development of treatments for vocal dysphonia has been inhibited by lack of human vocal fold (VF) mucosa models because of difficulty in procuring VF epithelial cells, epithelial cells’ limited proliferative capacity and absence of cell lines. Here we report development of engineered VF mucosae from hiPSC, transfected via TALEN constructs for green fluorescent protein, that mimic development of VF epithelial cells in utero. Modulation of FGF signaling achieves stratified squamous epithelium from definitive and anterior foregut derived cultures. Robust culturing of these cells on collagen-fibroblast constructs produces three-dimensional models comparable to in vivo VF mucosa. Furthermore, we demonstrate mucosal inflammation upon exposure of these constructs to 5% cigarette smoke extract. Upregulation of pro-inflammatory genes in epithelium and fibroblasts leads to aberrant VF mucosa remodeling. Collectively, our results demonstrate that hiPSC-derived VF mucosa is a versatile tool for future investigation of genetic and molecular mechanisms underlying epithelium-fibroblasts interactions in health and disease.
机译:缺乏人声折叠(VF)粘膜模型抑制了声音障碍的治疗,因为难以获得VF上皮细胞,上皮细胞的增殖能力有限以及缺乏细胞系。在这里,我们报道了从hiPSC中经工程改造的VF粘膜的发展,该过程通过TALEN构建体转染了绿色荧光蛋白,模仿子宫内VF上皮细胞的发育。 FGF信号的调节可从前肠和前肠前培养物中获得分层的鳞状上皮。将这些细胞在胶原成纤维细胞构建体上进行稳健培养可产生与体内VF粘膜相当的三维模型。此外,我们证明了这些结构暴露于5%的香烟烟雾提取物后的粘膜炎症。上皮和成纤维细胞中促炎基因的上调导致异常的VF粘膜重塑。总的来说,我们的结果表明,hiPSC衍生的VF粘膜是一种多功能工具,可用于进一步研究健康和疾病中上皮-成纤维细胞相互作用的遗传和分子机制。

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