Wu Xixi, Koch Marcus, Martínez Felipe P Perona, Schirhagl Romana, Włodarczyk-Biegun Małgorzata K
Department of Biomedical Engineering, University Medical Centre Groningen and University of Groningen, Ant. Deusinglaan 1, Groningen, 9713 AV, The Netherlands.
INM - Leibniz Institute for New Materials, Campus D2 2, 66123, Saarbruecken, Germany.
Small. 2024 Dec;20(49):e2403729. doi: 10.1002/smll.202403729. Epub 2024 Sep 9.
Skin equivalents (SE) that recapitulate biological and mechanical characteristics of the native tissue are promising platforms for assessing cosmetics and studying fundamental biological processes. Methods to achieve SEs with well-organized structure, and ideal biological and mechanical properties are limited. Here, the combination of melt electrowritten PCL scaffolds and cell-laden Matrigel to fabricate SE is described. The PCL scaffold provides ideal structural and mechanical properties, preventing deformation of the model. The model consists of a top layer for seeding keratinocytes to mimic the epidermis, and a bottom layer of Matrigel-based dermal compartment with fibroblasts. The compressive modulus and the biological properties after 3-day coculture indicate a close resemblance with the native skin. Using the SE, a testing system to study the damage caused by UVA irradiation and evaluate antioxidant efficacy is established. The effectiveness of Tea polyphenols (TPs) and L-ascorbic acid (Laa) is compared based on free radical generation. TPs are demonstrated to be more effective in downregulating free radical generation. Further, T1 relaxometry is used to detect the generation of free radicals at a single-cell level, which allows tracking of the same cell before and after UVA treatment.
能够重现天然组织生物学和力学特性的皮肤等效物(SE)是评估化妆品和研究基本生物学过程的有前景的平台。实现具有组织结构良好以及理想生物学和力学性能的SE的方法有限。在此,描述了将熔融电写聚己内酯(PCL)支架与载有细胞的基质胶相结合以制造SE的方法。PCL支架提供了理想的结构和力学性能,防止模型变形。该模型由用于接种角质形成细胞以模拟表皮的顶层和含有成纤维细胞的基于基质胶的真皮层组成。3天共培养后的压缩模量和生物学特性表明与天然皮肤非常相似。利用SE建立了一个研究紫外线A(UVA)辐射造成的损伤并评估抗氧化功效的测试系统。基于自由基生成比较了茶多酚(TPs)和L-抗坏血酸(Laa)的有效性。结果表明TPs在下调自由基生成方面更有效。此外,利用T1弛豫测量法在单细胞水平检测自由基的生成,这使得能够追踪UVA处理前后的同一细胞。