Synergistic anabolic actions of hyaluronic acid and platelet-rich plasma on cartilage regeneration in osteoarthritis therapy

被引:133
作者
Chen, Wei-Hong [1 ,2 ]
Lo, Wen-Cheng [3 ,4 ]
Hsu, Wei-Che [1 ,2 ]
Wei, Hong-Jian [1 ,2 ]
Liu, Hen-Yu [1 ,2 ]
Lee, Chian-Her [5 ]
Chen, Szu-Yu Tina [1 ,2 ]
Shieh, Ying-Hua [6 ]
Williams, David F. [7 ]
Deng, Win-Ping [1 ,2 ]
机构
[1] Taipei Med Univ, Stem Cell Res Ctr, Taipei 110, Taiwan
[2] Taipei Med Univ, Coll Oral, Grad Inst Biomed Mat & Engn, Taipei 110, Taiwan
[3] Taipei Med Univ Hosp, Dept Neurosurg, Taipei, Taiwan
[4] Taipei Med Univ, Sch Med, Taipei 110, Taiwan
[5] Taipei Med Univ Hosp, Orthopaed Res Ctr, Dept Orthopaed & Traumatol, Taipei, Taiwan
[6] Taipei Med Univ, Wan Fang Hosp, Dept Family Med, Taipei, Taiwan
[7] Wake Forest Inst Regenerat Med, Winston Salem, NC USA
关键词
Osteoarthritis (OA); Tissue regeneration; Anti-inflammation; Hyaluronic acid (HA); Platelet-rich plasma (PRP); RHEUMATOID-ARTHRITIS; INTRAARTICULAR INJECTION; INFLAMMATORY RESPONSE; EXTRACELLULAR-MATRIX; INTERVERTEBRAL DISC; ARTICULAR-CARTILAGE; GENE-EXPRESSION; CHONDROCYTES; CELLS; BLOOD;
D O I
10.1016/j.biomaterials.2014.07.058
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Osteoarthritis (OA) is a common disease associated with tissue inflammation, physical disability and imbalanced homeostasis in cartilage. For advanced treatments, biological approaches are currently focused on tissue regeneration and anti-inflammation. This study was undertaken to evaluate the therapeutic efficacies of hyaluronic acid (HA) and platelet-rich plasma (PRP) (HA+PRP) on OA. Articular chondrocytes were obtained from five OA patients. The optimal HA and PRP concentrations were evaluated by MTT assay. The expressions of chondrogenic and inflammatory genes were analyzed by RT-PCR. Signaling pathway was examined by immunoblotting and the expressions of OA pathology-related chemokines and cytokines was demonstrated by real-time PCR-based SuperArray. The therapeutic efficacies of HA+PRP were then demonstrated in 3D arthritic neo-cartilage and ACLT-OA model. Here we showed that HA+PRP could greatly retrieve pro-inflammatory cytokines-reduced articular chondrocytes proliferation and chondrogenic phenotypes, the mechanism of which involve the sequential activation of specific receptors CD44 and TGF-beta RII, downstream mediators Smad2/3 and Erk1/2, and the chondrogenic transcription factor SOX9. The real-time PCR-based SuperArray results also indicated that OA pathology-related chemokines and cytokines could be efficiently suppressed by HA+PRP. Moreover, the cartilaginous ECM could be retrieved from inflammation-induced degradation by HA+PRP in both 2D monolayer and 3D neo-cartilage model. Finally, the intra-articular injection of HA+PRP could strongly rescue the meniscus tear and cartilage breakdown and then decrease OA-related immune cells. The combination of HA+PRP can synergistically promote cartilage regeneration and inhibit OA inflammation. This study might offer an advanced and alternative OA treatment based on detailed regenerative mechanisms. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:9599 / 9607
页数:9
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