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Three-Dimensional Gastrointestinal Organoid Culture in Combination with Nerves or Fibroblasts: A Method to Characterize the Gastrointestinal Stem Cell Niche

机译:与神经或成纤维细胞结合的三维胃肠道类器官培养:表征胃肠干细胞小生境的一种方法

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The gastrointestinal epithelium is characterized by a high turnover of cells and intestinal stem cells predominantly reside at the bottom of crypts and their progeny serve to maintain normal intestinal homeostasis. Accumulating evidence demonstrates the pivotal role of a niche surrounding intestinal stem cells in crypts, which consists of cellular and soluble components and creates an environment constantly influencing the fate of stem cells. Here we describe different 3D culture systems to culture gastrointestinal epithelium that should enable us to study the stem cell nichein vitroin the future: organoid culture and multilayered systems such as organotypic cell culture and culture of intestinal tissue fragmentsex vivo. These methods mimic thein vivosituationin vitroby creating 3D culture conditions that reflect the physiological situation of intestinal crypts. Modifications of the composition of the culture media as well as coculturing epithelial organoids with previously described cellular components such as myofibroblasts, collagen, and neurons show the impact of the methods applied to investigate niche interactionsin vitro. We further present a novel method to isolate labeled nerves from the enteric nervous system using Dclk1-CreGFP mice.
机译:胃肠道上皮的特征是细胞的高周转率,而肠道干细胞主要位于隐窝的底部,它们的后代可维持正常的肠道稳态。越来越多的证据表明,隐窝周围小肠周围干细胞的利基作用至关重要,小隐窝由细胞和可溶性成分组成,并创造了一个不断影响干细胞命运的环境。在这里,我们描述了用于培养胃肠道上皮的不同3D培养系统,这将使我们能够在未来研究干细胞壁生蛋白:类器官培养和多层系统,例如有机型细胞培养和离体肠组织碎片的培养。这些方法通过创建反映肠道隐窝生理状况的3D培养条件来模仿体外体内情况。培养基组成的改变以及上皮类器官与先前描述的细胞成分如成肌纤维细胞,胶原蛋白和神经元的共培养显示了用于研究体外小生境相互作用的方法的影响。我们进一步提出了一种新的方法,使用Dclk1-CreGFP小鼠从肠神经系统中分离出标记神经。

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