Giardini-Rosa Renata, Joazeiro Paulo P, Thomas Kathryn, Collavino Kristina, Weber Joanna, Waldman Stephen D
1 Human Mobility Research Centre, Kingston General Hospital and Queen's University , Kingston, Canada .
Tissue Eng Part A. 2014 Mar;20(5-6):1012-26. doi: 10.1089/ten.TEA.2013.0159. Epub 2014 Jan 21.
External ear reconstruction with autologous cartilage still remains one of the most difficult problems in the fields of plastic and reconstructive surgery. As the absence of tissue vascularization limits the ability to stimulate new tissue growth, relatively few surgical approaches are currently available (alloplastic implants or sculpted autologous cartilage grafts) to repair or reconstruct the auricle (or pinna) as a result of traumatic loss or congenital absence (e.g., microtia). Alternatively, tissue engineering can offer the potential to grow autogenous cartilage suitable for implantation. While tissue-engineered auricle cartilage constructs can be created, a substantial number of cells are required to generate sufficient quantities of tissue for reconstruction. Similarly, as routine cell expansion can elicit negative effects on chondrocyte function, we have developed an approach to generate large-sized engineered auricle constructs (≥3 cm(2)) directly from a small population of donor cells (20,000-40,000 cells/construct). Using rabbit donor cells, the developed bioreactor-cultivated constructs adopted structural-like characteristics similar to native auricular cartilage, including the development of distinct cartilaginous and perichondrium-like regions. Both alterations in media composition and seeding density had profound effects on the formation of engineered elastic tissue constructs in terms of cellularity, extracellular matrix accumulation, and tissue structure. Higher seeding densities and media containing sodium bicarbonate produced tissue constructs that were closer to the native tissue in terms of structure and composition. Future studies will be aimed at improving the accumulation of specific tissue constituents and determining the clinical effectiveness of this approach using a reconstructive animal model.
自体软骨外耳重建仍然是整形和重建外科领域中最困难的问题之一。由于缺乏组织血管化限制了刺激新组织生长的能力,目前可用于修复或重建因创伤性缺失或先天性缺失(如小耳畸形)导致的耳廓(或耳郭)的手术方法相对较少(异体植入物或雕刻自体软骨移植物)。另外,组织工程学提供了生长适合植入的自体软骨的潜力。虽然可以创建组织工程化耳廓软骨构建体,但需要大量细胞才能产生足够数量的组织用于重建。同样,由于常规细胞扩增会对软骨细胞功能产生负面影响,我们开发了一种方法,可直接从小群供体细胞(20,000 - 40,000个细胞/构建体)生成大尺寸的工程化耳廓构建体(≥3 cm²)。使用兔供体细胞,开发的生物反应器培养构建体具有与天然耳廓软骨相似的结构特征,包括形成明显的软骨样和软骨膜样区域。培养基成分和接种密度的改变在细胞数量、细胞外基质积累和组织结构方面对工程化弹性组织构建体的形成都有深远影响。更高的接种密度和含有碳酸氢钠的培养基产生的组织构建体在结构和组成上更接近天然组织。未来的研究将致力于改善特定组织成分的积累,并使用重建动物模型确定该方法的临床有效性。