Rheumatology Advance Access originally published online on September 11, 2009
Rheumatology 2009 48(11):1447-1450; doi:10.1093/rheumatology/kep262
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Identification of phenotypic discriminating markers for intervertebral disc cells and articular chondrocytes
1INSERM (Institut National de la Santé et de la Recherche Médicale), U791, Osteoarticular and Dental Tissue Engineering Group, University of Nantes, 2Pharmacie Centrale, University Hospital of Nantes, 3UMR703-INRA, National Veterinary School, Développement et Pathologie du tissu Musculaire, 4Department of Neurosurgery, University Hospital of Nantes, Nantes, 5INSERM U747, University René Descartes, Paris and 6GRAFTYS SAS, Aix en Provence, France.
Correspondence to: Jérôme Guicheux, INSERM U791, Osteoarticular and Dental Tissue Engineering, University of Nantes, 1-Place Alexis Ricordeau, 44042, Nantes Cedex 1, France. E-mail: jerome.guicheux{at}inserm.fr
| Abstract |
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Objective. The present study was conducted to improve our knowledge of intervertebral disc (IVD) cell biology by comparing the phenotype of nucleus pulposus (NP) and annulus fibrosus (AF) cells with that of articular chondrocytes (ACs).
Methods. Rabbit cells from NP and AF were isolated and their phenotype was compared with that of AC by real-time PCR analysis of type I (COL1A1), II (COL2A1) and V (COL5A1) collagens, aggrecan transcript (AGC1), matrix Gla protein (MGP) and Htra serine peptidase 1 (Htra1).
Results. Transcript analysis indicated that despite certain similarities, IVD cells exhibit distinct COL2A1/COL1A1 and COL2A1/AGC1 ratios as compared with AC. The expression pattern of COL5A1, MGP and Htra1 makes it possible to define a phenotypic signature for NP and AF cells.
Conclusions. Our study shows that NP and AF cells exhibit a clearly distinguishable phenotype from that of AC. Type V collagen, MGP and HtrA1 could greatly help to discriminate among NP, AF and AC cells.
KEY WORDS: Intervertebral disc, Nucleus pulposus, Annulus fibrosus, Chondrocyte, Phenotype
Submitted 7 April 2009;
revised version accepted 22 July 2009.
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