Gotterbarm T, Breusch S J, Schneider U, Jung M
Department of Orthopaedic Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Lab Anim. 2008 Jan;42(1):71-82. doi: 10.1258/la.2007.06029e.
Articular cartilage repair is still a challenge in orthopaedic surgery. Although many treatment options have been developed in the last decade, true regeneration of hyaline articular cartilage is yet to be accomplished. In vitro experiments are useful for evaluating cell-matrix interactions under controlled parameters. When introducing new treatment options into clinical routine, adequate animal models are capable of closing the gap between in vitro experiments and the clinical use in human beings. We developed an animal model in the Göttingen minipig (GMP) to evaluate the healing of osteochondral or full-thickness cartilage defects. The defects were located in the middle third of the medial portion of the patellofemoral joint at both distal femurs. Chondral defects were 6.3 mm, osteochondral defects either 5.4 or 6.3 mm in diameter and 8 or 10 mm deep. In both defects the endogenous repair response showed incomplete repair tissue formation up to 12 months postoperatively. Based on its limited capability for endogenous repair of chondral and osteochondral defects, the GMP is a useful model for critical assessment of new treatment strategies in articular cartilage tissue engineering.
关节软骨修复在骨外科领域仍是一项挑战。尽管在过去十年中已开发出许多治疗方案,但透明关节软骨的真正再生尚未实现。体外实验有助于在可控参数下评估细胞与基质的相互作用。当将新的治疗方案引入临床常规时,合适的动物模型能够弥合体外实验与人类临床应用之间的差距。我们在哥廷根小型猪(GMP)中建立了一种动物模型,以评估骨软骨或全层软骨缺损的愈合情况。缺损位于双侧股骨远端髌股关节内侧部分的中三分之一处。软骨缺损直径为6.3毫米,骨软骨缺损直径为5.4或6.3毫米,深度为8或10毫米。在两种缺损中,内源性修复反应在术后12个月时均显示出不完全的修复组织形成。基于其对软骨和骨软骨缺损的内源性修复能力有限,GMP是用于严格评估关节软骨组织工程新治疗策略的有用模型。