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.

Highlights

  • Development of the protocolIt has been experimentally demonstrated that intestinal epithelial Caco-2 cells cultured in a gut-on-achip[1,2,3,4,5] or in a bilayered microfluidic device[6,7] can undergo spontaneous 3D morphogenesis in vitro without a clear understanding of the underlying mechanism

  • We identified that the removal of morphogen antagonists that are basolaterally secreted from the culture setup is necessary and sufficient to induce 3D epithelial morphogenesis in vitro, verified with both Caco-2 and patient-derived intestinal organoid epithelia[4]

  • We focused on the cellular production and concentration profile of a potent Wnt antagonist, Dickkopf-1 (DKK-1), in both guton-a-chip and a modified microfluidic device that contains a Transwell insert, called a ‘hybrid chip’

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Summary

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It has been experimentally demonstrated that intestinal epithelial Caco-2 cells cultured in a gut-on-achip[1,2,3,4,5] or in a bilayered microfluidic device[6,7] can undergo spontaneous 3D morphogenesis in vitro without a clear understanding of the underlying mechanism. 3D epithelial morphology may allow us to understand how the gut microbiota structures their communities and synergistically produces microbial metabolites (e.g., short-chain fatty acids) that shape the cellular organization and stem cell niche in the basal crypt These features can only be demonstrated when 3D epithelial layers are established in vitro. The nature of prestructured scaffolds may preclude demonstrating a spontaneous morphogenesis process per se These models do not offer dynamic luminal or interstitial flow, lacking fluid shear stress that intestinal cells need to undergo morphogenesis and gain physiological functions. Another recent study used a hydrogel scaffold in a microfluidic platform and patterned intestinal epithelial structure using a laser etching technology[31]. Our protocol for in vitro 3D morphogenesis may provide a complementary approach to overcome the challenges of the existing methods

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