用于生物发光报告基因检测的新型三维活皮肤样体外复合材料。

Tatsunosuke Tomita, Yoshihiro Nakajima, Yoshihiro Ohmiya, Koyomi Miyazaki
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引用次数: 0

摘要

我们对 HaCaT 细胞(一种自发永生的正常角质形成细胞系)进行了遗传操作,使其分别在白细胞介素 8(IL-8)和泛素-C(UBC)启动子的驱动下稳定表达两种不同颜色的荧光素酶报告基因。随后,我们利用这些细胞生成了三维(3D)类皮肤体外复合体(SLIC),目的是监测 SLIC 发出的生物荧光。这种三维类肤体外复合细胞是在分化培养基中的无纺硅纤维膜上生成的。对 SLIC 中皮肤分化标记物的免疫组化分析显示,角蛋白 2 和 10、丝胶蛋白和内卷曲素的表达表明了成熟皮肤的特征。这种工程化 SLIC 可用于实时生物发光监测,从而评估对紫外线压力以及亲水性和疏水性化学负荷的时间和剂量依赖性反应。值得注意的是,传统的二维细胞培养方法很难评估对疏水性物质的反应,这表明需要一种新方法,而这项技术可以解决这个问题。我们的观察结果表明,工程化 SLIC 具有由特定启动子驱动的组成型表达报告程序,可根据特定目标进行定制,极大地促进了基于遗传反应机制探索皮肤细胞生理功能的实验。它还为评估用于人体皮肤局部应用的各种化合物的生理影响提供了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Novel three-dimensional live skin-like in vitro composite for bioluminescence reporter gene assay.

We genetically manipulated HaCaT cells, a spontaneously immortalised normal keratinocyte cell line, to stably express two different coloured luciferase reporter genes, driven by interleukin 8 (IL-8) and ubiquitin-C (UBC) promoters, respectively. Subsequently, we generated a three-dimensional (3D) skin-like in vitro composite (SLIC) utilising these cells, with the objective of monitoring bioluminescence emitted from the SLIC. This SLIC was generated on non-woven silica fibre membranes in differentiation medium. Immunohistochemical analyses of skin differentiation markers in the SLIC revealed the expression of keratins 2 and 10, filaggrin, and involucrin, indicating mature skin characteristics. This engineered SLIC was employed for real-time bioluminescence monitoring, allowing the assessment of time- and dose-dependent responses to UV stress, as well as to hydrophilic and hydrophobic chemical loads. Notably, evaluation of responses to hydrophobic substances has been challenging with conventional 2D cell culture methods, suggesting the need for a new approach, which this technology could address. Our observations suggest that engineered SLIC with constitutively expressing reporters driven by selected promoters which are tailored to specific objectives, significantly facilitates assays exploring the physiological functions of skin cells based on genetic response mechanisms. It also highlights new avenues for evaluating the physiological impacts of various compounds designed for topical application to human skin.

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