Epidermis-on-a-chip system to develop skin barrier and melanin mimicking model

丝状蛋白 总苞素 表皮(动物学) 洛里克林 角蛋白 人体皮肤 生物医学工程 体外 细胞生物学 生物物理学 化学 材料科学 角质形成细胞 生物 解剖 病理 生物化学 免疫学 特应性皮炎 医学 遗传学
作者
Qiwei Li,Chunyan Wang,Xiaoran Li,Jing Zhang,Zilin Zhang,Keyu Yang,Jun Ouyang,Shaohui Zha,Lifeng Sha,Jianjun Ge,Zaozao Chen,Zhongze Gu
出处
期刊:Journal of Tissue Engineering [SAGE]
卷期号:14: 20417314231168529-20417314231168529 被引量:20
标识
DOI:10.1177/20417314231168529
摘要

In vitro skin models are rapidly developing and have been widely used in various fields as an alternative to traditional animal experiments. However, most traditional static skin models are constructed on Transwell plates without a dynamic three-dimensional (3D) culture microenvironment. Compared with native human and animal skin, such in vitro skin models are not completely biomimetic, especially regarding their thickness and permeability. Therefore, there is an urgent need to develop an automated biomimetic human microphysiological system (MPS), which can be used to construct in vitro skin models and improve bionic performance. In this work, we describe the development of a triple-well microfluidic-based epidermis-on-a-chip (EoC) system, possessing epidermis barrier and melanin-mimicking functions, as well as being semi-solid specimen friendly. The special design of our EoC system allows pasty and semi-solid substances to be effectively utilized in testing, as well as allowing for long-term culturing and imaging. The epidermis in this EoC system is well-differentiated, including basal, spinous, granular, and cornified layers with appropriate epidermis marker (e.g. keratin-10, keratin-14, involucrin, loricrin, and filaggrin) expression levels in corresponding layers. We further demonstrate that this organotypic chip can prevent permeation of over 99.83% of cascade blue (a 607 Da fluorescent molecule), and prednisone acetate (PA) was applied to test percutaneous penetration in the EoC. Finally, we tested the whitening effect of a cosmetic on the proposed EoC, thus demonstrating its efficacy. In summary, we developed a biomimetic EoC system for epidermis recreation, which could potentially serve as a useful tool for skin irritation, permeability, cosmetic evaluation, and drug safety tests.
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