Curcumin Supplementation Enhances Bone Marrow Mesenchymal Stem Cells to Promote the Anabolism of Articular Chondrocytes and Cartilage Repair

被引:22
|
作者
Zhang, Rui [1 ]
Zhang, Qiaoxia [2 ]
Zou, Zhiyu [1 ,3 ,4 ]
Li, Zheng [1 ,5 ]
Jin, Meng [1 ,6 ]
An, Jing [1 ]
Li, Hui [5 ]
Ma, Jianbing [5 ]
机构
[1] Xi An Jiao Tong Univ, Honghui Hosp, Translat Med Ctr, Xian 710054, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Basic Med, Hlth Sci Ctr, Xian, Shaanxi, Peoples R China
[3] Xi An Jiao Tong Univ, Honghui Hosp, Dept Integrated Tradit Chinese Med, Xian, Shaanxi, Peoples R China
[4] Xi An Jiao Tong Univ, Honghui Hosp, Western Med Orthopaed, Xian, Shaanxi, Peoples R China
[5] Xi An Jiao Tong Univ, Honghui Hosp, Dept Joint Surg, Xian, Shaanxi, Peoples R China
[6] Shannxi Univ Tradit Chinese Med, Sch Basic Med, Xian, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
curcumin; BMSCs; OA; chondrocytes; cartilage;
D O I
10.1177/0963689721993776
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Mesenchymal stem cells derived from bone marrows (BMSCs) and curcumin derived from turmeric were used for osteoarthritis (OA) treatment, respectively. We invested the effects of curcumin supplementation for BMSC therapeutic effects. In vitro, rat BMSCs were identified by dual-immunofluorescent staining of CD44 and CD90, and flow cytometry. Primary articular chondrocytes were identified by toluidine blue staining and immunofluorescent staining of Col2a1. EdU incorporation, migration assay, real-time quantitative polymerase chain reaction, and Western blot analyses were performed to evaluate the alterations of chondrocytes cocultured with BMSCs. In vivo, the rat model of OA was established by monoiodoacetic acid. After intra-articular injection of allogeneic BMSCs, articular cartilage damage and OA progression were evaluated by histological staining, and Osteoarthritis Research Society International and Mankin score evaluation. Although curcumin alone did not improve cell viability of primary articular chondrocytes, it promoted proliferation and migration of chondrocytes when cocultured with BMSCs. Meanwhile, the expression of anabolic genes in chondrocytes was remarkably increased both at mRNA and protein levels. In OA rats, curcumin and BMSCs cooperated to greatly promote articular cartilage repair and retard OA progression. Therefore, curcumin supplementation enhanced the BMSC function for the proliferation and migration of articular chondrocytes, and anabolic gene expression of extracellular matrix in articular chondrocytes in vitro, and the generation of articular cartilage in vivo. Our study shed light on the potential clinical application of curcumin cooperated with BMSCs in cartilage repair for OA treatment.
引用
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页数:12
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