Department of Dermatology, Leiden University Medical Centre, the Netherlands; Division of BioTherapeutics, Leiden Academic Centre for Drug Research, the Netherlands.
Division of BioTherapeutics, Leiden Academic Centre for Drug Research, the Netherlands.
J Steroid Biochem Mol Biol. 2019 May;189:19-27. doi: 10.1016/j.jsbmb.2019.01.022. Epub 2019 Jan 31.
Human skin equivalents (HSEs) are three dimensional models resembling native human skin (NHS) in many aspects. Despite the manifold similarities to NHS, a restriction in its applications is the altered in vitro lipid barrier formation, which compromises the barrier functionality. This could be induced by suboptimal cell culturing conditions, which amongst others is the diminished activation of the vitamin D receptor (VDR) signalling pathway. The active metabolite of this signalling pathway is 1,25-dihydroxyvitamin D (1,25(OH)D). An interacting role in the formation of the skin barrier has been ascribed to this pathway, although it remains unresolved to which extent this pathway contributes to the (mal-)formation of the epidermal barrier in HSEs. Our aim is to study whether cell culture medium enriched with 1,25(OH)D affects epidermal morphogenesis and lipid barrier formation in HSEs. Addition of 20 nM 1,25(OH)D resulted in activation of the VDR signalling pathway by inducing transcription of VDR target genes (CYP24A and LL37) in keratinocyte monocultures and in HSEs. Characterization of HSEs supplemented with 1,25(OH)D using immunohistochemical analyses revealed a high similarity in epidermal morphogenesis and in expression of lipid processing enzymes. The barrier formation was assessed using state-of-the art techniques analysing lipid composition and organization. Addition of 1,25(OH)D did not alter the composition of ceramides. Additionally, the lateral and lamellar organization of the lipids was similar, irrespective of supplementation. In conclusion, epidermal morphogenesis and barrier formation in HSEs generated in presence or absence of 1,25(OH)D leads to a similar morphogenesis and comparable barrier formation in vitro.
人体皮肤等效物(HSEs)是三维模型,在许多方面类似于天然人体皮肤(NHS)。尽管与 NHS 有许多相似之处,但它的应用受到限制,原因是体外脂质屏障形成发生改变,从而损害了屏障功能。这可能是由于细胞培养条件不理想所致,其中包括维生素 D 受体(VDR)信号通路的激活减弱。该信号通路的活性代谢物是 1,25-二羟基维生素 D(1,25(OH)D)。尽管该通路在皮肤屏障形成中的作用尚不清楚,但已有人指出该通路在形成皮肤屏障方面具有相互作用。我们的目的是研究富含 1,25(OH)D 的细胞培养基是否会影响 HSE 中的表皮形态发生和脂质屏障形成。在角质形成细胞的单核培养物和 HSE 中,添加 20 nM 1,25(OH)D 可通过诱导 VDR 靶基因(CYP24A 和 LL37)的转录来激活 VDR 信号通路。用免疫组织化学分析对补充了 1,25(OH)D 的 HSEs 进行表征,结果表明表皮形态发生和脂质处理酶的表达具有高度相似性。使用分析脂质组成和组织的最先进技术评估屏障形成。添加 1,25(OH)D 不会改变神经酰胺的组成。此外,无论是否补充,脂质的侧向和层状组织都相似。总之,在存在或不存在 1,25(OH)D 的情况下生成的 HSEs 的表皮形态发生和屏障形成导致体外相似的形态发生和可比的屏障形成。