Arévalo-Silva C A, Eavey R D, Cao Y, Vacanti M, Weng Y, Vacanti C A
Department of Otolaryngology, Massachusetts Eye and Ear Infirmary, 243 Charles St, Boston, MA 02114, USA.
Arch Otolaryngol Head Neck Surg. 2000 Dec;126(12):1448-52. doi: 10.1001/archotol.126.12.1448.
Auricles previously created by tissue engineering in nude mice used a biodegradable internal scaffold to maintain the desired shape of an ear. However, the biodegradable scaffold incited a compromising inflammatory response in subsequent experiments in immunocompetent animals.
To test the hypothesis that tissue-engineered autologous cartilage can be bioincorporated with a nonreactive, permanent endoskeletal scaffold.
Auricular elastic cartilage was harvested from Yorkshire swine. The chondrocytes were isolated and suspended into a hydrogel (Pluronic F-127) at a cell concentration of 5 x 10(7) cells/mL. Nonbiodegradable endoskeletal scaffolds were formed with 1 of 5 polymers: (1) high-density polyethylene, (2) soft acrylic, (3) polymethylmethacrylate, (4) extrapurified Silastic, and (5) conventional Silastic. Three groups were studied: (1) a control group using only the 5 polymers, (2) the 5 polymers enveloped by Pluronic F-127 only, and (3) the implants coated with Pluronic F-127 seeded with chondrocytes. All constructs were implanted subdermally; implants containing cells were implanted into the same animal from which the cells had been islolated. The implants were harvested after 8 weeks of in vivo culture and histologically analyzed.
Only implants coated by hydrogel plus cells generated healthy new cartilage. With 3 polymers (high-density polyethylene, acrylic, and extrapurified Silastic), the coverage was nearly complete by elastic cartilage, with minimal fibrocartilage and minimal to no inflammatory reaction. The Food and Drug Administration-approved conventional Silastic implants resulted in fragments of fibrous tissue mixed with elastic cartilage plus evidence of chronic inflammation. The polymethylmethacrylate implant was intermediate in the amount of cartilage formed and degree of inflammation.
This pilot technique combining tissue-engineered autologous elastic cartilage with a permanent biocompatible endoskeleton demonstrated success in limiting the inflammatory response to the scaffold, especially to high-density polyethylene, acrylic, and extrapurified Silastic. This model facilitates the potential to generate tissue of intricate shape, such as the human ear, by internal support. Arch Otolaryngol Head Neck Surg. 2000;126:1448-1452
先前在裸鼠体内通过组织工程构建的耳廓使用了可生物降解的内部支架来维持耳朵的理想形状。然而,在随后对具有免疫能力的动物进行的实验中,这种可生物降解支架引发了有害的炎症反应。
验证组织工程自体软骨能否与无反应的永久性内骨骼支架进行生物整合的假设。
从约克郡猪身上获取耳廓弹性软骨。分离软骨细胞并以5×10⁷个细胞/毫升的细胞浓度悬浮于水凝胶(普朗尼克F - 127)中。用5种聚合物中的1种形成不可生物降解的内骨骼支架:(1)高密度聚乙烯,(2)软质丙烯酸树脂,(3)聚甲基丙烯酸甲酯,(4)超纯化硅橡胶,(5)传统硅橡胶。研究了三组:(1)仅使用5种聚合物的对照组,(2)仅被普朗尼克F - 127包裹的5种聚合物,(3)涂有普朗尼克F - 127并接种软骨细胞的植入物。所有构建体均皮下植入;含有细胞的植入物植入到分离出细胞的同一动物体内。体内培养8周后取出植入物并进行组织学分析。
只有水凝胶加细胞涂层的植入物产生了健康的新软骨。对于3种聚合物(高密度聚乙烯、丙烯酸树脂和超纯化硅橡胶),弹性软骨的覆盖几乎完全,纤维软骨极少,炎症反应轻微至无。美国食品药品管理局批准的传统硅橡胶植入物导致纤维组织碎片与弹性软骨混合,并伴有慢性炎症迹象。聚甲基丙烯酸甲酯植入物形成的软骨量和炎症程度处于中间水平。
这种将组织工程自体弹性软骨与永久性生物相容性内骨骼相结合的初步技术成功地限制了对支架的炎症反应,尤其是对高密度聚乙烯、丙烯酸树脂和超纯化硅橡胶的炎症反应。该模型有助于通过内部支撑生成复杂形状组织(如人耳)的潜力。《耳鼻喉头颈外科档案》。2000年;126:1448 - 1452