Teng Margie S, Yuen Audrey S, Kim Hubert T
Stanford University School of Medicine, Stanford, CA, USA.
Clin Orthop Relat Res. 2008 Aug;466(8):1804-9. doi: 10.1007/s11999-008-0302-8. Epub 2008 May 28.
Osteochondral allograft transplantation is a well-accepted treatment for articular cartilage damage. However, chondrocyte viability declines during graft storage, which may compromise graft performance. We first tested the hypothesis that the composition of commonly used storage media affects the viability of articular chondrocytes over time; we then tested the hypothesis that the addition of insulin growth factor-1 or the apoptosis inhibitor ZVAD-fmk could enhance the storage properties of serum-free media. Bovine osteochondral grafts were stored at 4 degrees C in lactated Ringer's, Dulbecco's modified eagle's media (DMEM), DMEM supplemented with either insulin growth factor-1 or ZVAD-fmk, and a commercial storage media. Chondrocyte viability in lactated Ringer's declined rapidly to 20.4% at 2 weeks. Viability in DMEM declined more slowly to 54.8% at 2 weeks and 31.2% at 3 weeks. Viability in commercial storage media was 83.6% at 3 weeks and 44.8% at 4 weeks. Viability was increased in DMEM + insulin growth factor-1 (56.4%) and DMEM + ZVAD (52.4%) at 3 weeks compared with DMEM alone. These results confirm the hypotheses that media composition greatly influences chondrocyte viability during cold storage and that insulin growth factor-1 and ZVAD improve the storage properties of DMEM.
异体骨软骨移植是一种被广泛接受的治疗关节软骨损伤的方法。然而,移植物储存期间软骨细胞活力会下降,这可能会影响移植物的性能。我们首先测试了常用储存培养基的成分是否会随时间影响关节软骨细胞活力这一假设;然后测试了添加胰岛素生长因子-1或凋亡抑制剂ZVAD-fmk是否能增强无血清培养基储存特性的假设。牛骨软骨移植物在4℃下分别储存于乳酸林格氏液、杜氏改良伊格尔培养基(DMEM)、添加胰岛素生长因子-1或ZVAD-fmk的DMEM以及一种商业储存培养基中。乳酸林格氏液中的软骨细胞活力在2周时迅速降至20.4%。DMEM中的活力下降较慢,2周时降至54.8%,3周时降至31.2%。商业储存培养基中的活力在3周时为83.6%,4周时为44.8%。与单独的DMEM相比,3周时DMEM +胰岛素生长因子-1组(56.4%)和DMEM + ZVAD组(52.4%)的活力有所增加。这些结果证实了以下假设:培养基成分在冷藏期间对软骨细胞活力有很大影响,并且胰岛素生长因子-1和ZVAD可改善DMEM的储存特性。