Orthopaedic Research Laboratories, Department of Orthopaedic Surgery, University of Virginia Health System, Charlottesville, Virginia 22908, USA.
Tissue Eng Part A. 2010 Sep;16(9):2941-51. doi: 10.1089/ten.tea.2009.0710.
Adipose-derived mesenchymal stem cells (ADMSCs) are a unique population of stem cells with therapeutic potential in the treatment of connective tissue injuries. Growth differentiation factor-5 (GDF)-5 is known to play a role in tendon repair and maintenance. The aim of this study was to investigate the effects of GDF-5 on proliferation and tendonogenic gene expression of rat ADMSCs.
ADMSCs were treated in culture with different concentrations of GDF-5 (0-1000 ng/mL) for 12 days. Biochemical, temporal, and concentration kinetic studies were done. Extracellular matrix (ECM) synthesis, tendonogenic differentiation, and matrix remodeling gene and protein expression were analyzed.
GDF-5 led to increased ADMSC proliferation in a dose- and time-dependent manner. ADMSCs demonstrated enhanced ECM (collagen type I, decorin, and aggrecan) and tendonogenic marker (scleraxis, tenomodulin, and tenascin-C) gene expression with 100 ng/mL of GDF-5 (p < 0.05). ECM and tendon-specific markers showed time-dependent increases at various time points (p < 0.05), although decorin decreased at day 9 (p < 0.05). GDF-5 did alter expression of matrix remodeling genes, with no specific trends observed. Western blot analysis confirmed dose- and time-dependent increases in protein expression of tenomodulin, tenascin-C, Smad-8, and matrix metalloproteinase-13.
In vitro GDF-5 treatment can induce cellular events leading to the tendonogenic differentiation of ADMSCs. The use of combined GDF-5 and ADMSCs tissue-engineered therapies may have a role in the future of tendon repair.
脂肪间充质干细胞(ADMSCs)是一种具有治疗潜力的独特干细胞群体,可用于治疗结缔组织损伤。生长分化因子 5(GDF-5)在肌腱修复和维持中起作用。本研究旨在探讨 GDF-5 对大鼠 ADMSCs 增殖和肌腱发生基因表达的影响。
ADMSCs 在不同浓度的 GDF-5(0-1000ng/ml)中培养 12 天。进行了生化、时程和浓度动力学研究。分析细胞外基质(ECM)合成、肌腱发生分化和基质重塑基因和蛋白表达。
GDF-5 以剂量和时间依赖的方式导致 ADMSC 增殖增加。ADMSCs 表现出增强的 ECM(I 型胶原、核心蛋白聚糖和聚集蛋白聚糖)和肌腱发生标记物(肌腱蛋白聚糖、肌腱调蛋白和腱生蛋白-C)基因表达,浓度为 100ng/ml 的 GDF-5(p<0.05)。在不同时间点,ECM 和肌腱特异性标记物呈时间依赖性增加(p<0.05),尽管核心蛋白聚糖在第 9 天减少(p<0.05)。GDF-5 确实改变了基质重塑基因的表达,但没有观察到特定的趋势。Western blot 分析证实,肌腱调蛋白、腱生蛋白-C、Smad-8 和基质金属蛋白酶-13 的蛋白表达呈剂量和时间依赖性增加。
体外 GDF-5 处理可诱导细胞事件,导致 ADMSCs 的肌腱发生分化。联合 GDF-5 和 ADMSCs 组织工程疗法的应用可能在未来的肌腱修复中发挥作用。