Autologous Adipose-Derived Mesenchymal Stem Cells Combined with Shockwave Therapy Synergistically Ameliorates the Osteoarthritic Pathological Factors in Knee Joint.
Jai-Hong ChengKe-Tien YenWen-Yi ChouShun-Wun JhanShan-Ling HsuJih-Yang KoChing-Jen WangChun-En Aurea KuoSzu-Ying WuTsai-Chin HsuChieh-Cheng HsuPublished in: Pharmaceuticals (Basel, Switzerland) (2021)
Adipose-derived mesenchymal stem cells (ADSCs) and shockwave (SW) therapy have been shown to exert a chondroprotective effect for osteoarthritis (OA). The results of this study demonstrated that autologous ADSCs had dose-dependent and synergistic effects with SW therapy (0.25 mJ/mm2 with 800 impulses) in OA rat knee joint. Autologous, high-dose 2 × 106 ADSCs (ADSC2 group) combined with SW therapy significantly increased the bone volume, trabecular thickness, and trabecular number among in the treatment groups. ADSC2 combined with SW therapy significantly reduced the synovitis score and OARSI score in comparison with other treatments. In the analysis of inflammation-induced extracellular matrix factors of the articular cartilage in OA, the results displayed that ADSC2 combined with SW therapy had a greater than other treatments in terms of reducing tumor necrosis factor-inducible gene (TSG)-6 and proteoglycan (PRG)-4, in addition to increasing tissue inhibitor matrix metalloproteinase (TIMP)-1 and type II collagen. Furthermore, ADSC2 combined with SW therapy significantly reduced the expression of inflammation-induced bone morphogenetic protein (BMP)-2 and BMP-6. Therefore, the results demonstrated that ADSC2 combined with SW therapy had a synergistic effect to ameliorate osteoarthritic pathological factors in OA joints.
Keyphrases
- mesenchymal stem cells
- oxidative stress
- high dose
- bone marrow
- extracellular matrix
- cell therapy
- type diabetes
- gene expression
- low dose
- metabolic syndrome
- bone mineral density
- optical coherence tomography
- dna methylation
- skeletal muscle
- high glucose
- knee osteoarthritis
- endothelial cells
- drug delivery
- long non coding rna
- bone regeneration
- binding protein
- soft tissue
- chemotherapy induced