Department of Orthopaedic Surgery, Graduate School of Biomedical & Health Sciences, Hiroshima University, Kasumi, Minami-ku, Hirosima-shi, Hiroshima, Japan.
Am J Sports Med. 2019 Jul;47(9):2216-2224. doi: 10.1177/0363546519854372. Epub 2019 Jun 17.
Autologous chondrocyte implantation (ACI) is often performed for large cartilage defects. Because this technique has several disadvantages, including the need for second-stage surgery, cartilage repair using minced cartilage has been suggested. However, this technique could be improved using 3-dimensional scaffolds.
To examine the ability of chondrocyte migration and proliferation from minced cartilage in atelocollagen gel in vitro and evaluate the repairable potential of minced cartilage embedded in atelocollagen gel covered with a periosteal flap in a rabbit model.
Controlled laboratory study.
Minced cartilage or isolated chondrocytes from rabbits were embedded in atelocollagen gel and cultured for 3 weeks. Chondrocyte proliferation and matrix production were evaluated in vitro. An osteochondral defect at the trochlear groove was created in 56 rabbits, which were divided into 4 groups. The defect was left empty (defect group), filled with allogenic minced cartilage (minced cartilage group), filled with isolated allogenic chondrocytes embedded in atelocollagen gel (ACI group), or filled with atelocollagen gel (atelocollagen with periosteal flap group). At 4, 12, and 24 weeks after surgery, repair of the defect was evaluated in these 4 groups.
In vitro, the number of chondrocytes and abundant matrix on the surface of the gel significantly increased in the minced cartilage group compared with the ACI group ( < .05). In vivo, the minced cartilage and ACI groups showed good cartilage repair compared with the empty defect and atelocollagen/periosteal flap groups ( < .05); there was no significant difference in the Pineda score between the minced cartilage and ACI groups.
Minced cartilage in atelocollagen gel had good chondrocyte migration and proliferation abilities in vitro, and osteochondral defects were well repaired by implanting minced cartilage embedded in the atelocollagen gel in vivo. Implantation of minced cartilage embedded in atelocollagen gel showed good cartilage repair equivalent to ACI.
Implantation of minced cartilage embedded in atelocollagen gel as a 1-step procedure has outcomes similar to those of ACI but is cheaper and more convenient than ACI.
自体软骨细胞移植(ACI)常用于治疗大的软骨缺损。由于该技术存在需要二期手术等多种缺点,因此有人提出使用碎软骨进行软骨修复。然而,这种技术可以通过三维支架得到改善。
在体外检查纤维连接蛋白凝胶中碎软骨的软骨细胞迁移和增殖能力,并评估在骨膜瓣覆盖的纤维连接蛋白凝胶中嵌入碎软骨的兔模型的可修复潜力。
对照实验室研究。
将兔碎软骨或分离的软骨细胞嵌入纤维连接蛋白凝胶中培养 3 周。体外评估软骨细胞增殖和基质产生情况。在 56 只兔子的滑车沟处造成骨软骨缺损,将其分为 4 组。缺损处为空(缺损组),填充同种异体碎软骨(碎软骨组),填充嵌入纤维连接蛋白凝胶的同种异体分离软骨细胞(ACI 组),或填充纤维连接蛋白凝胶(纤维连接蛋白/骨膜瓣组)。术后 4、12 和 24 周,对这 4 组的缺损修复情况进行评估。
体外研究中,与 ACI 组相比,碎软骨组的软骨细胞数量和凝胶表面丰富的基质明显增加(<0.05)。体内研究中,与空缺损和纤维连接蛋白/骨膜瓣组相比,碎软骨和 ACI 组的软骨修复良好(<0.05);碎软骨和 ACI 组的 Pineda 评分无显著差异。
体外纤维连接蛋白凝胶中的碎软骨具有良好的软骨细胞迁移和增殖能力,体内植入嵌入纤维连接蛋白凝胶中的碎软骨可很好地修复骨软骨缺损。植入嵌入纤维连接蛋白凝胶的碎软骨显示出与 ACI 相当的良好软骨修复效果。
作为一步法,将嵌入纤维连接蛋白凝胶的碎软骨植入具有与 ACI 相似的结果,但比 ACI 更经济、更方便。