Laboratory for Wound Healing Repair and Regenerative Medicine, Department of Surgery, Division of Plastic and Reconstructive Surgery, Northwestern University, Feinberg School of Medicine, Chicago, IL, USA.
Lab Invest. 2012 Apr;92(4):584-99. doi: 10.1038/labinvest.2011.184. Epub 2012 Jan 9.
A number of in vivo and ex vivo skin models have been applied to human wound healing studies. A reliable skin model, which recapitulates the features of human wound repair, is essential for the clinical and mechanical investigation of human cutaneous wound healing. Full-skin ex vivo culture systems have been used in wound healing studies. However, important structures of the skin, such as the differentiation of keratinocytes and epidermis-dermis junction, are poorly characterized in this model. This study aims to develop an optimized partial-thickness human ex vivo skin culture (HESC) model to maintain human skin characteristics in vitro. During our culture, the basal layer, suprabasal layer, and stratum granulosum layer of epidermis were preserved until day 8. Analyses of hemidesmosome proteins, bullous pemphigoid antigen 1 (BP180) and 2 (BP230), showed that the integrity of the basement membrane of the epidermis was well preserved in the HESC model. In contrast, an organotypic culture with human keratinocytes and fibroblasts failed to show an integrated basement membrane. Maintenance of skin structure by histological analysis and proliferation of epidermal keratinocytes by Ki67 staining were observed in our model for 12 days. Complete re-epithelialization of the wounding area was observed at day 6 post wounding when a superficial incisional wound was created. The expression of Ki-67 and keratin 6, indicators of activated keratinocytes in epidermis, was significantly upregulated and new collagen synthesis was found in the dermis during the wound healing process. As control, we also used organotypic culture in studying the differentiation of the keratinocyte layers and incisional wound repair. It turned out that our model has advantage in these study fields. The results suggest that our HESC model retains important elements of in vivo skin and has significant advantages for the wound healing studies in vitro.
多种体内和体外皮肤模型已被应用于人类伤口愈合研究。一种可靠的皮肤模型,能够重现人类伤口修复的特征,对于人类皮肤伤口愈合的临床和机械研究至关重要。全皮肤离体培养系统已被用于伤口愈合研究。然而,该模型中皮肤的重要结构,如角质形成细胞的分化和表皮-真皮连接,特征描述较差。本研究旨在开发一种优化的部分厚度人离体皮肤培养(HESC)模型,以维持体外人类皮肤特征。在我们的培养过程中,表皮的基底层、上基底层和颗粒层一直保留到第 8 天。表皮半桥粒蛋白、大疱性类天疱疮抗原 1(BP180)和 2(BP230)的分析表明,HESC 模型中表皮基底膜的完整性得到了很好的保留。相比之下,人角质形成细胞和成纤维细胞的器官型培养未能显示出完整的基底膜。我们的模型在 12 天内通过组织学分析观察到皮肤结构的维持和表皮角质形成细胞的增殖,通过 Ki67 染色观察到 6 天的浅层切开伤后伤口区域的完全再上皮化。Ki-67 和角蛋白 6 的表达明显上调,表明表皮中角质形成细胞被激活,真皮中发现新的胶原蛋白合成,这是伤口愈合过程中的指标。作为对照,我们还使用器官型培养来研究角质形成细胞层的分化和切开伤修复。结果表明,我们的模型在这些研究领域具有优势。结果表明,我们的 HESC 模型保留了体内皮肤的重要元素,并且在体外伤口愈合研究中具有显著优势。