Center of Experimental Orthopaedics, Saarland University Medical Center, Homburg/Saar, Germany.
Department of Orthopaedic Surgery, Saarland University Medical Center, Homburg/Saar, Germany.
J Cell Mol Med. 2017 Nov;21(11):2748-2758. doi: 10.1111/jcmm.13190. Epub 2017 May 3.
Implantation of peripheral blood aspirates induced towards chondrogenic differentiation upon genetic modification in sites of articular cartilage injury may represent a powerful strategy to enhance cartilage repair. Such a single-step approach may be less invasive than procedures based on the use of isolated or concentrated MSCs, simplifying translational protocols in patients. In this study, we provide evidence showing the feasibility of overexpressing the mitogenic and pro-anabolic insulin-like growth factor I (IGF-I) in human peripheral blood aspirates via rAAV-mediated gene transfer, leading to enhanced proliferative and chondrogenic differentiation (proteoglycans, type-II collagen, SOX9) activities in the samples relative to control (reporter rAAV-lacZ) treatment over extended periods of time (at least 21 days, the longest time-point evaluated). Interestingly, IGF-I gene transfer also triggered hypertrophic, osteo- and adipogenic differentiation processes in the aspirates, suggesting that careful regulation of IGF-I expression may be necessary to contain these events in vivo. Still, the current results demonstrate the potential of targeting human peripheral blood aspirates via therapeutic rAAV transduction as a novel, convenient tool to treat articular cartilage injuries.
通过基因修饰,将外周血抽吸物在关节软骨损伤部位向软骨分化诱导植入,可能代表一种增强软骨修复的有力策略。与基于分离或浓缩 MSC 使用的程序相比,这种一步法可能侵入性更小,简化了患者的转化方案。在这项研究中,我们提供了证据,表明通过 rAAV 介导的基因转移在外周血抽吸物中过表达有丝分裂原和促合成代谢的胰岛素样生长因子 I (IGF-I) 的可行性,相对于对照(报告 rAAV-lacZ)处理,这导致样本中的增殖和软骨分化(糖胺聚糖、II 型胶原、SOX9)活性增强,延长时间(至少 21 天,评估的最长时间点)。有趣的是,IGF-I 基因转移也触发了抽吸物中的肥大、骨和脂肪分化过程,表明在体内有必要对 IGF-I 表达进行仔细调节以抑制这些事件。尽管如此,目前的结果表明,通过治疗性 rAAV 转导靶向人外周血抽吸物作为一种新的、方便的治疗关节软骨损伤的工具具有潜力。