Institute of Biomedical Engineering, Chinese Academy of Medical Sciences, Peking Union Medical College, The Key Laboratory of Biomedical Material of Tianjin, Tianjin 300192, PR China.
School of Chemistry and Chemical Engineering, Tianjin University of Technology, Tianjin 300384, PR China.
Acta Biomater. 2018 Mar 15;69:170-182. doi: 10.1016/j.actbio.2018.01.039. Epub 2018 Feb 2.
It is reported that growth factor (GF) is able to enhance the repair of articular cartilage (AC) defect, however underlying mechanisms of which are not fully elucidated yet. Moreover, the strategy for delivering GF needs to be optimized. The crosstalk between AC and subchondral bone (SB) play important role in the homeostasis and integrity of AC, therefore SB targeted delivery of GF represents one promising way to facilitate the repair of AC defect. In this study, we firstly investigated the effects and mechanism of FGF2 on surrounding SB and cartilage of detect defects in rabbits by using a homogenous collagen-based membranes. It was found that FGF2 had a modulating effect on the defect-surrounding SB via upregulation of bone morphogenetic protein (BMP)-2, BMP4 and SOX9 at the early stage. Low dose FGF2 improved the repair upon directly injected to SB. Inhibition of BMP signaling pathway compromised the beneficial effects of FGF2, which indicated the pivotal roles of BMP in the process. To facilitate SB targeted FGF2 delivery, a double-layered inhomogeneous collagen membrane was prepared and it induced increase of BMP2 and BMP4 in the synovial fluid, and subsequent successful repair of AC defect. Taken together, this targeted delivery of FGF2 to SB provides a promising strategy for AC repair owing to the relatively clear mechanism, less amount of it, and short duration of delivery.
Articular cartilage (AC) and subchondral bone (SB) form an integral functional unit. The homeostasis and integrity of AC depend on its crosstalk with the SB. However, the function of the SB in AC defect repair is not completely understood. The application of growth factors to promote the repair articular cartilage defect is a promising strategy, but still under the optimization. Our study demonstrate that SB plays important roles in the repair of AC defect. Particularly, SB is the effective target of fibroblast growth factor 2 (FGF2), and targeted delivery of FGF2 can modulate SB and thus significantly enhances the repair of AC defect. Therefore, targeted delivery of growth factor to SB is a novel promising strategy to improve the repair of AC defect.
据报道,生长因子(GF)能够增强关节软骨(AC)缺损的修复,但其中的潜在机制尚未完全阐明。此外,GF 的输送策略需要优化。AC 和软骨下骨(SB)之间的相互作用在 AC 的稳态和完整性中起着重要作用,因此,针对 SB 的 GF 靶向输送是促进 AC 缺损修复的一种很有前途的方法。在这项研究中,我们首先使用均质胶原膜研究了 FGF2 对兔 AC 缺损周围 SB 和软骨的影响和机制。结果发现,FGF2 通过早期上调骨形态发生蛋白(BMP)-2、BMP4 和 SOX9 对周围 SB 具有调节作用。低剂量 FGF2 直接注射到 SB 中可改善修复效果。BMP 信号通路的抑制削弱了 FGF2 的有益作用,这表明 BMP 在该过程中起着关键作用。为了促进针对 SB 的 FGF2 输送,制备了双层不均匀胶原膜,它诱导滑液中 BMP2 和 BMP4 的增加,并随后成功修复了 AC 缺损。总之,由于相对明确的机制、较少的量和较短的输送时间,将 FGF2 靶向输送到 SB 为 AC 修复提供了一种很有前途的策略。
关节软骨(AC)和软骨下骨(SB)形成一个完整的功能单元。AC 的稳态和完整性依赖于其与 SB 的相互作用。然而,SB 在 AC 缺损修复中的作用尚未完全理解。应用生长因子促进关节软骨缺损的修复是一种很有前途的策略,但仍在优化中。我们的研究表明,SB 在 AC 缺损修复中起着重要作用。特别是,SB 是成纤维细胞生长因子 2(FGF2)的有效靶点,FGF2 的靶向输送可以调节 SB,从而显著增强 AC 缺损的修复。因此,将生长因子靶向输送到 SB 是一种改善 AC 缺损修复的新的很有前途的策略。