Orthopaedic Research Laboratories, Department of Orthopaedic Surgery, University of Virginia, Charlottesville, VA 22908, USA.
J Tissue Eng Regen Med. 2011 Mar;5(3):191-200. doi: 10.1002/term.304.
The synthesis and organization of extracellular matrix (ECM) of tendon, in resting and states of repair, are governed by fibroblasts. Growth differentiation factor-5 (GDF-5) may enhance the cellular response to tendon injury, thus improving the structural outcome of the regenerative tissue. This study was an attempt to identify potential mechanisms controlling the response of fibroblasts to injury and GDF-5, in the pursuit of improved tissue regeneration. There were two sets of experiments. Isolated mice Achilles tendon fibroblasts were treated with different concentrations of rGDF-5 (0-100 ng/ml) for 0-12 days in cell culture. The temporal effect of rGDF-5 on ECM gene expression was analysed for type I collagen and aggrecan expression. Microarray and gene expression analysis were performed on cells treated with 100 ng/ml for 4 days. Forty-five mice underwent bilateral mid-substance Achilles tendon tenotomy and suture repair. Repair sites were injected with 10 µg rGDF-5 or saline. Tendons were assessed histologically at 2, 4 and 6 weeks. Expression of ECM genes procollagen IX, aggrecan, matrix metalloproteinase 9 and fibromodulin were upregulated. Proinflammatory reaction genes were downregulated. rGDF-5 led to an increase in total DNA, glycosaminoglycan (GAG) and hydroxyproline (OHP). The OHP:DNA ratio of fibroblast cultures was increased over all time points, with increased GAG:DNA at day 12. rGDF-5 treatment showed improved collagen organization over controls. The results delineate the mode of action of rGDF-5 at the cellular and gene level. rGDF-5 could play a role in tendon repair and be used for future therapies that promote tendon healing.
肌腱细胞外基质(ECM)的合成和组织在静息和修复状态下受成纤维细胞调控。生长分化因子-5(GDF-5)可能增强细胞对肌腱损伤的反应,从而改善再生组织的结构结果。本研究试图确定控制成纤维细胞对损伤和 GDF-5 反应的潜在机制,以追求改善组织再生。有两组实验。在细胞培养中,用不同浓度的 rGDF-5(0-100ng/ml)处理分离的小鼠跟腱成纤维细胞 0-12 天。分析 rGDF-5 对 I 型胶原和聚集蛋白聚糖表达的时间效应。用 100ng/ml 处理 4 天的细胞进行微阵列和基因表达分析。45 只小鼠进行双侧跟腱中段切开和缝合修复。修复部位注射 10μg rGDF-5 或生理盐水。在 2、4 和 6 周时评估肌腱的组织学。细胞外基质基因前胶原 IX、聚集蛋白聚糖、基质金属蛋白酶 9 和纤维调节素的表达上调。促炎反应基因下调。rGDF-5 导致总 DNA、糖胺聚糖(GAG)和羟脯氨酸(OHP)增加。成纤维细胞培养物的 OHP:DNA 比值在所有时间点均升高,12 天时 GAG:DNA 增加。rGDF-5 处理显示胶原组织比对照组更有序。结果描述了 rGDF-5 在细胞和基因水平上的作用模式。rGDF-5 可能在肌腱修复中发挥作用,并可用于未来促进肌腱愈合的治疗方法。