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Therapeutic Benefit for Late, but Not Early, Passage Mesenchymal Stem Cells on Pain Behaviour in an Animal Model of Osteoarthritis.
Chapman, Victoria; Markides, Hareklea; Sagar, Devi Rani; Xu, Luting; Burston, James J; Mapp, Paul; Kay, Alasdair; Morris, Robert H; Kehoe, Oksana; El Haj, Alicia J.
Afiliação
  • Chapman V; Arthritis Research UK Pain Centre and School of Life Sciences, University of Nottingham, Nottingham, UK.
  • Markides H; Institute for Science and Technology in Medicine, Guy Hilton Research Centre, Keele University, Staffordshire, UK.
  • Sagar DR; Arthritis Research UK Pain Centre and School of Life Sciences, University of Nottingham, Nottingham, UK.
  • Xu L; Arthritis Research UK Pain Centre and School of Life Sciences, University of Nottingham, Nottingham, UK.
  • Burston JJ; Arthritis Research UK Pain Centre and School of Life Sciences, University of Nottingham, Nottingham, UK.
  • Mapp P; Arthritis Research UK Pain Centre and School of Life Sciences, University of Nottingham, Nottingham, UK.
  • Kay A; Institute for Science and Technology in Medicine, Keele University at RJAH Orthopaedic Hospital, Oswestry, UK.
  • Morris RH; School of Science and Technology, Nottingham Trent University, Nottingham, UK.
  • Kehoe O; Institute for Science and Technology in Medicine, Keele University at RJAH Orthopaedic Hospital, Oswestry, UK.
  • El Haj AJ; Institute for Science and Technology in Medicine, Guy Hilton Research Centre, Keele University, Staffordshire, UK.
Stem Cells Int ; 2017: 2905104, 2017.
Article em En | MEDLINE | ID: mdl-29434641
ABSTRACT

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 × 106 late passage MSCs labelled with 10 µg/ml SiMAG, 1.5 × 106 late passage mesenchymal stem cells, the steroid Kenalog (200 µg/20 µL), 1.5 × 106 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.

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Stem Cells Int Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Stem Cells Int Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Reino Unido