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Generation of organized anterior foregut epithelia from pluripotent stem cells using small molecules

机译:使用小分子从多能干细胞中产生有组织的前肠前皮

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摘要

Anterior foregut endoderm (AFE) gives rise to therapeutically relevant cell types in tissues such as the esophagus, salivary glands, lung, thymus, parathyroid and thyroid. Despite its importance, reports describing the generation of AFE from pluripotent stem cells (PSCs) by directed differentiation have mainly focused on the Nkx2.1~+ lung and thyroid lineages. Here, we describe a novel protocol to derive a subdomain of AFE, identified by expression of Pax9, from PSCs using small molecules and defined media conditions. We generated a reporter PSC line for isolation and characterization of Pax9~+ AFE cells, which when transplanted in vivo, can form several distinct complex AFE-derived epithelia, including mucosal glands and stratified squamous epithelium. Finally, we show that the directed differentiation protocol can be used to generate AFE from human PSCs. Thus, this work both broadens the range of PSC-derived AFE tissues and creates a platform enabling the study of AFE disorders.
机译:前肠内胚层(AFE)在诸如食道,唾液腺,肺,胸腺,甲状旁腺和甲状腺等组织中产生与治疗相关的细胞类型。尽管它很重要,但有关通过定向分化从多能干细胞(PSC)产生AFE的报道主要集中在Nkx2.1〜+肺和甲状腺谱系上。在这里,我们描述了一种新颖的协议,可以使用小分子和定义的培养基条件,从PSC衍生出通过Pax9表达鉴定的AFE子域。我们生成了一个记者PSC系,用于Pax9〜+ AFE细胞的分离和鉴定,当体内移植时,它可以形成几种不同的,复杂的AFE衍生上皮,包括粘膜腺和分层的鳞状上皮。最后,我们表明定向分化协议可用于从人PSC生成AFE。因此,这项工作既拓宽了PSC衍生的AFE组织的范围,又创造了一个平台,能够研究AFE疾病。

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