L'Oréal Research & Innovation, Clichy, France.
Tissue Eng Part C Methods. 2012 Dec;18(12):947-57. doi: 10.1089/ten.TEC.2011.0676. Epub 2012 Jul 2.
To study human skin pigmentation in a physiological in vitro model, we developed a pigmented reconstructed skin reproducing the three-dimensional architecture of the melanocyte environment and the interactions of melanocyte with its cellular partners, keratinocytes, and fibroblasts. Co-seeding melanocytes and keratinocytes onto a fibroblast-populated collagen matrix led to a correct integration of melanocytes within the epidermal basal layer, but melanocytes remained amelanotic even after supplementation with promelanogenic factors. Interestingly, normalization of keratinocyte differentiation using keratinocyte growth factor instead of epidermal growth factor finally allowed an active pigmentary system to develop, as shown by the expression of key melanogenic markers, the production, and transfer of melanosome-containing melanin into keratinocytes. Various degrees of constitutive pigmentation were reproduced using melanocytes from different skin phenotypes. Furthermore, induction of pigmentation was achieved by treatment with known propigmenting molecules, αMSH and forskolin, thus demonstrating the functionality of the pigmentary system. This pigmented full-thickness skin model therefore represents a highly relevant tool to study the role of cell-cell, cell-matrix, and mesenchymal-epithelial interactions in the control of skin pigmentation.
为了在生理体外模型中研究人类皮肤色素沉着,我们开发了一种着色的重建皮肤,再现了黑素细胞环境的三维结构以及黑素细胞与其细胞伴侣角质形成细胞和成纤维细胞的相互作用。将黑素细胞和角质形成细胞共同接种到成纤维细胞 populate 的胶原基质上,导致黑素细胞正确地整合到表皮基底层中,但即使补充了促黑素生成因子,黑素细胞仍然呈无色素沉着状态。有趣的是,使用角质形成细胞生长因子而不是表皮生长因子来使角质形成细胞分化正常化,最终使一个活跃的色素生成系统得以发育,如关键黑素生成标志物的表达、黑色素体含有黑色素的产生和转移到角质形成细胞中所示。使用来自不同皮肤表型的黑素细胞再现了不同程度的组成性色素沉着。此外,通过用已知的促色素生成分子 αMSH 和 forskolin 处理来诱导色素沉着,从而证明了色素生成系统的功能。因此,这种着色的全厚皮肤模型代表了一种非常相关的工具,可用于研究细胞-细胞、细胞-基质和间充质-上皮相互作用在皮肤色素沉着控制中的作用。