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Enhancing Osteochondral Allograft Viability: Effects of Storage Media Composition

机译:增强骨软骨移植的生存力:存储介质组成的影响。

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摘要

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°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.
机译:骨软骨移植是关节软骨损伤的公认方法。但是,软骨细胞的活力在移植物储存期间下降,这可能会损害移植物的性能。我们首先检验了以下假设:常用存储介质的组成会随着时间的推移影响关节软骨细胞的生存能力。然后我们检验了以下假设:添加胰岛素生长因子-1或凋亡抑制剂ZVAD-fmk可以增强无血清培养基的储存性能。牛骨软骨移植物在4°C下储存在乳酸林格氏液,Dulbecco改良的Eagle培养基(DMEM),补充有胰岛素生长因子1或ZVAD-fmk的DMEM以及市售储存介质中。乳酸林格氏液中的软骨细胞活力在2周时迅速下降至20.4%。 DMEM的活力在2周时下降至54.8%,在3周时下降至31.2%。商业存储介质在3周时的生存率为83.6%,在4周时为44.8%。与仅使用DMEM相比,在3周时DMEM +胰岛素生长因子-1(56.4%)和DMEM + ZVAD(52.4%)的活力增加。这些结果证实了以下假设:培养基成分在冷藏期间会严重影响软骨细胞的活力,胰岛素生长因子-1和ZVAD会改善DMEM的贮藏性能。

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