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) sk...

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Veröffentlicht in:The FEBS journal 2024-10, Vol.291 (20), p.4619-4632
Hauptverfasser: Tomita, Tatsunosuke, Nakajima, Yoshihiro, Ohmiya, Yoshihiro, Miyazaki, Koyomi
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Sprache:eng
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Zusammenfassung: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. We engineered HaCaT cells to stably express promoter‐regulated luciferase reporter genes. Using these cells, we then generated a 3D skin‐like in vitro composite (SLIC) with the aim of monitoring bioluminescence emitted in response to UV or chemical triggers in real time. In addition to overcoming the challenges associated with testing hydrophobic compounds using traditional 2D culture methods, this is a useful model for exploring the physiological functions of skin cells in specific genetic contexts and can be further utilised for testing various compounds.
ISSN:1742-464X
1742-4658
1742-4658
DOI:10.1111/febs.17246