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在具有细胞培养插入物的肠道芯片或混合芯片中,人类肠道上皮细胞的 3D 体外形态发生。

3D in vitro morphogenesis of human intestinal epithelium in a gut-on-a-chip or a hybrid chip with a cell culture insert.

机构信息

Department of Biomedical Engineering, The University of Texas at Austin, Austin, TX, USA.

Wyss Institute for Biologically Inspired Engineering at Harvard University, Boston, MA, USA.

出版信息

Nat Protoc. 2022 Mar;17(3):910-939. doi: 10.1038/s41596-021-00674-3. Epub 2022 Feb 2.

DOI:10.1038/s41596-021-00674-3
PMID:35110737
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9675318/
Abstract

Human intestinal morphogenesis establishes 3D epithelial microarchitecture and spatially organized crypt-villus characteristics. This unique structure is necessary to maintain intestinal homeostasis by protecting the stem cell niche in the basal crypt from exogenous microbial antigens and their metabolites. Also, intestinal villi and secretory mucus present functionally differentiated epithelial cells with a protective barrier at the intestinal mucosal surface. Thus, re-creating the 3D epithelial structure is critical to building in vitro intestine models. Notably, an organomimetic gut-on-a-chip can induce spontaneous 3D morphogenesis of an intestinal epithelium with enhanced physiological function and biomechanics. Here we provide a reproducible protocol to robustly induce intestinal morphogenesis in a microfluidic gut-on-a-chip as well as in a Transwell-embedded hybrid chip. We describe detailed methods for device fabrication, culture of Caco-2 or intestinal organoid epithelial cells in conventional setups as well as on microfluidic platforms, induction of 3D morphogenesis and characterization of established 3D epithelium using multiple imaging modalities. This protocol enables the regeneration of functional intestinal microarchitecture by controlling basolateral fluid flow within 5 d. Our in vitro morphogenesis method employs physiologically relevant shear stress and mechanical motions, and does not require complex cellular engineering or manipulation, which may be advantageous over other existing techniques. We envision that our proposed protocol may have a broad impact on biomedical research communities, providing a method to regenerate in vitro 3D intestinal epithelial layers for biomedical, clinical and pharmaceutical applications.

摘要

人类肠道形态发生建立了 3D 上皮微结构和空间组织的隐窝-绒毛特征。这种独特的结构对于维持肠道内稳态至关重要,它可以保护基底隐窝中的干细胞龛免受外源性微生物抗原及其代谢物的影响。此外,肠道绒毛和分泌性粘液呈现出具有功能分化的上皮细胞,在肠黏膜表面形成保护屏障。因此,重建 3D 上皮结构对于构建体外肠道模型至关重要。值得注意的是,类器官肠道芯片可以诱导肠道上皮的自发 3D 形态发生,增强其生理功能和生物力学特性。在这里,我们提供了一个可重复的方案,以在微流控肠芯片和 Transwell 嵌入式混合芯片中稳健地诱导肠道形态发生。我们详细描述了设备制造、常规设置和微流控平台上 Caco-2 或肠类器官上皮细胞培养、3D 形态发生诱导以及使用多种成像模式对已建立的 3D 上皮组织进行特征描述的方法。该方案可通过控制基底外侧流体流动在 5 天内再生功能性肠道微结构。我们的体外形态发生方法采用了生理相关的剪切应力和机械运动,且不需要复杂的细胞工程或操作,这可能优于其他现有的技术。我们设想,我们提出的方案可能会对生物医学研究社区产生广泛的影响,为生物医学、临床和制药应用提供了一种再生体外 3D 肠道上皮层的方法。

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