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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.
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页码:1085 / 1096
页数:12
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