Staudenmaier Rainer, Hoang T Nguyen, Kleinsasser Norbert, Schurr Christian, Frölich Kathrin, Wenzel Magdalene M, Aigner Joachim
ENT Department, University of Regensburg Hospital, Regensburg, Germany.
J Reconstr Microsurg. 2004 Oct;20(7):555-64. doi: 10.1055/s-2004-836127.
In reconstructive surgery, the integration of tissue-engineered cartilage in a prefabricated free flap may make it possible to generate flaps combining a variety of tissue components, to meet the special requirements of particular defects. One aim of the present study was to investigate prefabrication of a microvascular free flap by implanting a vessel loop under a skin flap in a rabbit model. A second aim was to report on the authors' preliminary experiences in prelaminating prefabricated flaps with autologous tissue-engineered cartilage, in terms of matrix development, inflammatory reaction, and host-tissue interaction. The flap was prefabricated by implanting a vessel loop under a random-pattern abdominal skin flap. The tissue-engineered cartilage constructs were made by isolating chondrocytes from auricular biopsies. Following a period of amplification, the cells were seeded onto a non-woven scaffold made of a hyaluronic-acid derivative and cultivated for 2 weeks. One cell-biomaterial construct was placed beneath the prefabicated flap, and two additional constructs were placed subcutaneously and intramuscularly. In addition, a biomaterial sample without cells was placed subcutaneously to provide a control. All implanted specimens were left in position for 6 or 12 weeks. Neovascularization in the prefabricated flap and biomaterial construct was analyzed by angiography. After explantation, the specimens were examined by histologic and immunohistochemical methods. The prefabricated flaps showed a well-developed network of blood vessels between the implanted vessel loop and the original random-pattern blood supply. The tissue-engineered constructs remained stable in size and showed signs of tissue similar to hyaline cartilage, as evidenced by the expression of cartilage-specific collagen type II and proteoglycans. No inflammatory reactions were observed. The physiologic environment of the autologous rabbit model provided favorable conditions for matrix deposition and maturation of the cell-biomaterial constructs. These initial results demonstrated the potential of prefabricating an axial perfused flap, combined with tissue-engineered cartilage, thus creating functionally competent tissue components for reconstructive surgery with minimal donor-site morbidity.
在重建外科手术中,将组织工程化软骨整合到预制游离皮瓣中,可能使生成结合多种组织成分的皮瓣成为可能,以满足特定缺损的特殊要求。本研究的一个目的是在兔模型中通过在皮瓣下植入血管袢来研究微血管游离皮瓣的预制。另一个目的是报告作者在将预制皮瓣与自体组织工程化软骨进行预分层方面在基质发育、炎症反应和宿主组织相互作用方面的初步经验。通过在随意型腹部皮瓣下植入血管袢来预制皮瓣。组织工程化软骨构建体通过从耳廓活检中分离软骨细胞制成。经过一段时间的扩增后,将细胞接种到由透明质酸衍生物制成的无纺支架上并培养2周。将一个细胞 - 生物材料构建体置于预制皮瓣下方,另外两个构建体分别置于皮下和肌肉内。此外,将无细胞的生物材料样本置于皮下作为对照。所有植入标本放置6或12周。通过血管造影分析预制皮瓣和生物材料构建体中的新血管形成。取出后,通过组织学和免疫组织化学方法检查标本。预制皮瓣在植入的血管袢和原始随意型血供之间显示出发育良好的血管网络。组织工程构建体在大小上保持稳定,并显示出类似于透明软骨的组织迹象,软骨特异性II型胶原蛋白和蛋白聚糖的表达证明了这一点。未观察到炎症反应。自体兔模型的生理环境为细胞 - 生物材料构建体的基质沉积和成熟提供了有利条件。这些初步结果证明了预制轴向灌注皮瓣并结合组织工程化软骨的潜力,从而为重建手术创造功能健全的组织成分,同时使供区发病率降至最低。