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在平面和成型胶原水凝胶上体外生成自我更新的人类肠道上皮。

In vitro generation of self-renewing human intestinal epithelia over planar and shaped collagen hydrogels.

机构信息

Department of Bioengineering, University of Washington, Seattle, WA, USA.

出版信息

Nat Protoc. 2021 Jan;16(1):352-382. doi: 10.1038/s41596-020-00419-8. Epub 2020 Dec 9.

Abstract

The large intestine, with its array of crypts lining the epithelium and diverse luminal contents, regulates homeostasis throughout the body. In vitro crypts formed from primary human intestinal epithelial stem cells on a 3D shaped hydrogel scaffold replicate the functional and architectural features of in vivo crypts. Collagen scaffolding assembly methods are provided, along with the microfabrication and soft lithography protocols necessary to shape these hydrogels to match the dimensions and density of in vivo crypts. In addition, stem-cell scale-up protocols are provided so that even ultrasmall primary samples can be used as starting material. Initially, these cells are seeded as a proliferative monolayer over the shaped scaffold and cultured as stem/proliferative cells to expand them and cover the scaffold surface with the crypt-shaped structures. To convert these immature crypts into fully polarized, functional units with a basal stem cell niche and luminal differentiated cell zone, stable, linear gradients of growth factors are formed across the crypts. This platform supports the formation of chemical gradients across the crypts, including those of growth and differentiation factors, inflammatory compounds, bile and food metabolites and bacterial products. All microfabrication and device assembly steps are expected to take 8 d, with the primary cells cultured for 12 d to form mature in vitro crypts.

摘要

大肠,其上皮衬里的一系列隐窝和多样化的腔内容物,调节着全身的内稳态。从三维形状的水凝胶支架上的原代人肠道上皮干细胞形成的体外隐窝复制了体内隐窝的功能和结构特征。提供了胶原支架组装方法,以及微制造和软光刻协议,这些协议用于将这些水凝胶塑造成与体内隐窝的尺寸和密度相匹配的形状。此外,还提供了干细胞扩大方案,以便即使是非常小的原始样本也可以用作起始材料。最初,这些细胞作为增殖单层接种在成型支架上,并作为干细胞/增殖细胞培养以扩大它们,并使隐窝状结构覆盖支架表面。为了将这些不成熟的隐窝转化为具有基底干细胞龛和腔分化细胞区的完全极化、功能单位,在隐窝中形成稳定的、线性的生长因子梯度。该平台支持跨隐窝形成化学梯度,包括生长和分化因子、炎症化合物、胆汁和食物代谢物以及细菌产物的梯度。所有微制造和器件组装步骤预计需要 8 天,原代细胞培养 12 天以形成成熟的体外隐窝。

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