Cell Therapy With G-CSF-Mobilized Stem Cells in a Rat Osteoarthritis Model

被引:23
|
作者
Deng, Ming-Wei [1 ]
Wei, Shih-Jung [2 ]
Yew, Tu-Lai [3 ]
Lee, Po-Hui [4 ]
Yang, Tzu-Yu [2 ]
Chu, Hen-Yi [1 ]
Hung, Shih-Chieh [2 ,5 ,6 ,7 ,8 ]
机构
[1] Enhance Biomed Ltd, Taipei, Taiwan
[2] Taipei Vet Gen Hosp, Dept Med Res & Educ, Stem Cell Lab, Taipei 11217, Taiwan
[3] Natl Yang Ming Univ, Dept Biotechnol & Lab Sci Med, Taipei 112, Taiwan
[4] Natl Yang Ming Univ, Inst Oral Biol, Taipei 112, Taiwan
[5] Taipei Vet Gen Hosp, Dept Orthopaed & Traumatol, Taipei 11217, Taiwan
[6] Natl Yang Ming Univ, Inst Clin Med, Taipei 112, Taiwan
[7] Natl Yang Ming Univ, Inst Pharmacol, Taipei 112, Taiwan
[8] Acad Sinica, Inst Biomed Sci, Taipei, Taiwan
关键词
Granulocyte colony-stimulating factor; Osteoarthritis; Peripheral blood stem cells; Autologous; Preclinical trial; PERIPHERAL-BLOOD; BONE-MARROW; PROGENITOR CELLS; CARTILAGE; DIFFERENTIATION; POPULATION; KNEE; COLLECTION; OCT-4(+); DEFECTS;
D O I
10.3727/096368914X680091
中图分类号
Q813 [细胞工程];
学科分类号
摘要
G-CSF-mobilized peripheral blood stem cells (gm-PBSCs) offer a convenient cell source for treatment of hematopoietic and vascular disorders. Whether gm-PBSCs provide beneficial effects on skeleton diseases, such as osteoarthritis (OA), remains unknown. This study was undertaken to address the hypothesis that gm-PBSCs promote articular regeneration in OA. Here we studied the effect of single-dose intra-articular injection of gm-PBSCs from male donors delivered in hyaluronic acid (HA) on papain-induced OA in the knee joints of female Sprague Dawley (SD) rats. Contralateral OA knee joints received single-dose HA alone and served as vehicle controls. We evaluated the histologic changes in glycosarninoglycan, type II collagen, type X collagen, modified Mankin score, and cell apoptosis rate in the articular cartilage of rat knees. We demonstrated that gm-PBSCs were mobilized to the peripheral blood via G-CSF infusion for 5 days in SD rats with increasing CD34(+) percentage up to 55-fold. We showed that gm-PBSCs inhibit progression of papain-induced OA via reducing articular surface irregularity, fibrillation, and erosion, preventing cellular necrosis and loss of chondrogenic proteins, such as glycosaminoglycan and type II collagen, at both 3 and 6 weeks after treatment. Moreover, gm-PBSCs reduced modified Mankin scores and cellular apoptosis rates compared with HA alone. Our findings demonstrate that HA plus gm-PBSCs, rather than HA alone, inhibits progression of OA in rats in vivo. Thus, intra-articular injection of gm-PBSCs is a convenient protocol for treating OA with consistent beneficial effects.
引用
收藏
页码:1085 / 1096
页数:12
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