Therapeutic Benefit for Late, but Not Early, Passage Mesenchymal Stem Cells on Pain Behaviour in an Animal Model of Osteoarthritis

被引:19
作者
Chapman, Victoria [1 ,2 ]
Markides, Hareklea [3 ]
Sagar, Devi Rani [1 ,2 ]
Xu, Luting [1 ,2 ]
Burston, James J. [1 ,2 ]
Mapp, Paul [1 ,2 ]
Kay, Alasdair [4 ]
Morris, Robert H. [5 ]
Kehoe, Oksana [4 ]
El Haj, Alicia J. [3 ]
机构
[1] Univ Nottingham, Arthrit Res UK Pain Ctr, Nottingham, England
[2] Univ Nottingham, Sch Life Sci, Nottingham, England
[3] Keele Univ, Guy Hilton Res Ctr, Inst Sci & Technol Med, Keele, Staffs, England
[4] Keele Univ, RJAH Orthopaed Hosp, Inst Sci & Technol Med, Oswestry, Shrops, England
[5] Nottingham Trent Univ, Sch Sci & Technol, Nottingham, England
基金
英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
BONE-MARROW; RHEUMATOID-ARTHRITIS; KNEE OSTEOARTHRITIS; RAT MODEL; INTRAARTICULAR INJECTION; PROLIFERATION KINETICS; PROGENITOR CELLS; STROMAL CELLS; TRACKING; CULTURE;
D O I
10.1155/2017/2905104
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background. Mesenchymal stem cells (MSCs) have a therapeutic potential for the treatment of osteoarthritic (OA) joint pathology and pain. The aims of this study were to determine the influence of a passage number on the effects of MSCs on pain behaviour and cartilage and bone features in a rodent model of OA. Methods. Rats underwent either medial meniscal transection (MNX) or sham surgery under anaesthesia. Rats received intra-articular injection of either 1.5 x 10(6) late passage MSCs labelled with 10 mu g/ml SiMAG, 1.5 x 10(6) late passage mesenchymal stem cells, the steroid Kenalog (200 mu g/20 mu L), 1.5 x 10(6) early passage MSCs, or serum-free media (SFM). Sham-operated rats received intra-articular injection of SFM. Pain behaviour was quantified until day 42 postmodel induction. Magnetic resonance imaging (MRI) was used to localise the labelled cells within the knee joint. Results. Late passage MSCs and Kenalog attenuated established pain behaviour in MNX rats, but did not alter MNX-induced joint pathology at the end of the study period. Early passage MSCs exacerbated MNX-induced pain behaviour for up to one week postinjection and did not alter joint pathology. Conclusion. Our data demonstrate for the first time the role of a passage number in influencing the therapeutic effects of MSCs in a model of OA pain.
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页数:11
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