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首页> 外文期刊>In Vitro Cellular and Developmental Biology. Animal: Journal of the Tissues Culture Association >Air-liquid and liquid-liquid interfaces influence the formation of the urothelial permeability barrier in vitro
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Air-liquid and liquid-liquid interfaces influence the formation of the urothelial permeability barrier in vitro

机译:气液界面和液液界面影响体外尿路上皮渗透屏障的形成

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Optimizing culture conditions is known to be crucial for the differentiation of urothelial cell cultures and the formation of the permeability barrier. However, so far, no data exist to confirm if air-liquid (AL) and liquid-liquid (LL) interfaces are physiologically relevant during urothelial differentiation and barrier formation. To reveal the influence of interfaces on the proliferation, differentiation, and barrier formation of the urothelial cells (UCs) in vitro, we cultured UCs under four different conditions, i.e., at the AL or LL interfaces with physiological calcium concentration and without serum or without physiological calcium concentration and with serum. For each of the four models, the urothelial integrity was tested by measuring the transepithelial resistance (TER), and the differentiation stage was examined by immunolabeling of differentiation-related markers and ultrastructural analysis. We found that the UCs at a LL interface, regardless of the presence or absence of calcium or serum, form the urothelium with more cell layers and achieve a higher TER than UCs at an AL interface. However, UCs grown at an AL interface with physiological concentration of calcium in medium form only one- to two-layered urothelium of UCs, which are larger and express more differentiation-related proteins uroplakins than UCs in other models. These results demonstrate that the interface itself can play a major, although so-far neglected, role in urothelial physiology, particularly in the formation of the urothelial permeability barrier in vitro and the regulatory mechanisms related with urothelial differentiation. In the study, the culturing of UCs in three successive steps is proposed.
机译:已知优化培养条件对于尿路上皮细胞培养物的分化和通透性屏障的形成至关重要。但是,到目前为止,尚无数据可确定尿液上皮分化和屏障形成过程中气液(AL)和液液(LL)界面在生理上是否相关。为了揭示界面对体外尿路上皮细胞(UCs)增殖,分化和屏障形成的影响,我们在四种不同条件下培养了UC,即在具有生理钙浓度且无血清或无血清的AL或LL界面生理钙浓度并与血清。对于这四个模型中的每个模型,通过测量跨上皮抵抗性(TER)来测试尿道上皮的完整性,并通过分化相关标记物的免疫标记和超微结构分析来检查分化阶段。我们发现,无论是否存在钙或血清,LL接口处的UCs形成的尿路上皮具有更多的细胞层,并且比AL接口处的UCs具有更高的TER。但是,在AL界面上生长的UC与培养基中的钙的生理浓度仅形成一到两层的UCs尿路上皮,与其他模型中的UC相比,UCs更大且表达更多的分化相关蛋白尿素激酶。这些结果表明,界面本身可以在尿路上皮生理学中发挥主要作用(尽管到目前为止已被忽略),尤其是在体外形成尿路上皮渗透性屏障以及与尿路上皮分化相关的调节机制中。在研究中,提出了连续三个步骤培养UC的方法。

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