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Alterations of overused supraspinatus tendon: A possible role of glycosaminoglycans and HARP/pleiotrophin in early tendon pathology
Authors:Mohamed Attia  Alexander Scott  Arlette Duchesnay  Gilles Carpentier  Louis J. Soslowsky  Minh Bao Huynh  Toin H. Van Kuppevelt  Camille Gossard  José Courty  Marie‐Claude Tassoni  Isabelle Martelly
Affiliation:1. Laboratoire CRRET CNRS EAC 7149, Université Paris‐Est Créteil, 61 Av du Général de Gaulle, 94010 Créteil Cedex, France;2. Cogitobio, Département de mécanobiologie, Cachan, France;3. Department of Physical Therapy, Centre for Hip Health and Mobility, University of British Columbia, Vancouver, BC, Canada;4. McKay Orthopaedic Research Laboratory, University of Pennsylvania, Philadelphia, Pennsylvania;5. The Department of Biochemistry, Radboud University Nijmegen Medical Centre, Nijmegen Centre for Molecular Life Sciences, Nijmegen, The Netherlands;6. Osteobio, Ecole Supérieure d'Ostéopathie et de Biomécanique Appliquée, Cachan, France
Abstract:Supraspinatus tendon overuse injuries lead to significant pain and disability in athletes and workers. Despite the prevalence and high social cost of these injuries, the early pathological events are not well known. We analyzed the potential relation between glycosaminoglycan (GAG) composition and phenotypic cellular alteration using a rat model of rotator cuff overuse. Total sulfated GAGs increased after 4 weeks of overuse and remained elevated up to 16 weeks. GAG accumulation was preceded by up‐regulation of decorin, versican, and aggrecan proteoglycans (PGs) mRNAs and proteins and biglycan PG mRNA after 2 weeks. At 2 weeks, collagen 1 transcript decreased whereas mRNAs for collagen 2, collagen 3, collagen 6, and the transcription factor Sox9 were increased. Protein levels of heparin affine regulatory peptide (HARP)/pleiotrophin, a cytokine known to regulate developmental chondrocyte formation, were enhanced especially at 4 weeks, without up‐regulation of HARP/pleiotrophin mRNA. Further results suggest that the increased GAGs present in early lesions may sequester HARP/pleiotrophin, which could contribute to a loss of tenocyte's phenotype. All these modifications are characteristic of a shift towards the chondrocyte phenotype. Identification of these early changes in the extra‐cellular matrix may help to prevent the progression of the pathology to more disabling, degenerative alterations. © 2011 Orthopaedic Research Society Published by Wiley Periodicals, Inc. J Orthop Res 30:61–71, 2012
Keywords:supraspinatus tendon  proteoglycans  glycosaminoglycans  chondrogenesis  HARP/pleiotrophin
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