La bone sialoproteine: un facteur clé dans la pathogénie de l'arthrosePesesse, Laurence ; Sanchez, Christelle ; et alConference (2012, December) Detailed reference viewed: 1 (0 ULg) Association entre l'hypertrophie du chondrocyte et l'angiogenèse du cartilage dans l'arthrosePesesse, Laurence ; Sanchez, Christelle ; et alConference (2012, December) Detailed reference viewed: 14 (1 ULg) Association between chondrocytes hypertrophy and angiogenesis of cartilage in osteoarthritisPesesse, Laurence ; Sanchez, Christelle ; et alPoster (2012, November 13) Detailed reference viewed: 11 (1 ULg) Association between chondrocytes hypertrophy and angiogenesis of cartilage in osteoarthritisPesesse, Laurence ; Sanchez, Christelle ; et alin Arthritis and Rheumatism (2012, October), 64(10 (Suppl)), 760 Detailed reference viewed: 21 (3 ULg) Bone sialoprotein: a key mediator of the angiogenic activity of hypertrophic osteoarthritic chondrocytesPesesse, Laurence ; Sanchez, Christelle ; et alPoster (2012, April) Detailed reference viewed: 14 (0 ULg) Bone sialoprotein: a key mediator of the angiogenic activity of hypertrophic osteoarthritic chondrocytesPesesse, Laurence ; Sanchez, Christelle ; et alin Osteoarthritis and Cartilage (2012), 20(S), 122-123 Detailed reference viewed: 6 (0 ULg) Association entre l'hypertrophie du chondrocyte et l'angiogenèse du cartilage dans l'arthrosePesesse, Laurence ; Sanchez, Christelle ; et alin Revue du Rhumatisme (2012), 79(S), 105-106 Detailed reference viewed: 2 (0 ULg) La bone sialoproteine: un facteur clé dans la pathogénie de l'arthrosePesesse, Laurence ; Sanchez, Christelle ; et alin Revue du Rhumatisme (2012), 79(S), 106 La bone sialoproteine: un facteur clé dans la pathogénie de l'arthrosePesesse, Laurence ; Sanchez, Christelle ; et alin Revue du Rhumatisme (2012), 79(S), 106 Regulation of subchondral bone osteoblast metabolism by cyclic compression.Sanchez, Christelle ; Pesesse, Laurence ; et alin Arthritis and Rheumatism (2012), 64(4), 1193-203 OBJECTIVE: Recent data have shown that abnormal subchondral bone remodeling plays an important role in osteoarthritis (OA) onset and progression, and it was suggested that abnormal mechanical pressure ... [more ▼] OBJECTIVE: Recent data have shown that abnormal subchondral bone remodeling plays an important role in osteoarthritis (OA) onset and progression, and it was suggested that abnormal mechanical pressure applied to the articulation was responsible for these metabolic changes. This study was undertaken to evaluate the effects of cyclic compression on osteoblasts from OA subchondral bone. METHODS: Osteoblasts were isolated from sclerotic and nonsclerotic areas of human OA subchondral bone. After 28 days, the osteoblasts were surrounded by an abundant extracellular matrix and formed a resistant membrane, which was submitted to cyclic compression (1 MPa at 1 Hz) for 4 hours. Gene expression was evaluated by reverse transcription-polymerase chain reaction. Protein production in culture supernatants was quantified by enzyme-linked immunosorbent assay or visualized by immunohistochemistry. RESULTS: Compression increased the expression of genes coding for interleukin-6 (IL-6), cyclooxygenase 2, RANKL, fibroblast growth factor 2, IL-8, matrix metalloproteinase 3 (MMP-3), MMP-9, and MMP-13 but reduced the expression of osteoprotegerin in osteoblasts in both sclerotic and nonsclerotic areas. Colalpha1(I) and MMP-2 were not significantly affected by mechanical stimuli. Nonsclerotic osteoblasts were significantly more sensitive to compression than sclerotic ones, but after compression, differences in messenger RNA levels between nonsclerotic and sclerotic osteoblasts were largely reduced or even abolished. Under basal conditions, sclerotic osteoblasts expressed similar levels of alpha5, alphav, beta1, and beta3 integrins and CD44 as nonsclerotic osteoblasts but 30% less connexin 43, an important mechanoreceptor. CONCLUSION: Genes involved in subchondral bone sclerosis are mechanosensitive. After compression, nonsclerotic and sclerotic osteoblasts expressed a similar phenotype, suggesting that compression could be responsible for the phenotype changes in OA subchondral osteoblasts. [less ▲] Detailed reference viewed: 24 (1 ULg) La Bone sialoprotéine est associée à la différenciation hypertrophique des chondrocytes et aux lésions du cartilage arthrosiquePesesse, Laurence ; Sanchez, Christelle ; et alin Revue du Rhumatisme (2011), 78(suppl 5), 99-100 Detailed reference viewed: 19 (2 ULg) La Bone sialoprotéine est associée à la différenciation hypertrophique des chondrocytes et aux lésions du cartilage arthrosiquePesesse, Laurence ; Sanchez, Christelle ; et alConference (2011) Detailed reference viewed: 16 (3 ULg) Study of the association between bone sialoprotein, hypertrophic differentiation of chondrocytes and cartilage lesions in osteoarthritic cartilagePesesse, Laurence ; Sanchez, Christelle ; et alin Osteoarthritis and Cartilage (2011), 19(Suppl 1), 106 Detailed reference viewed: 8 (0 ULg) Matrix metalloproteinase-3 is a highly mechanosensitive gene in human subchondral osteoblastsSanchez, Christelle ; Pesesse, Laurence ; et alin Osteoarthritis and Cartilage (2010), 17(suppl 2), 217 Detailed reference viewed: 25 (2 ULg) Effects of compression on human subchondral osteoblast metabolismKesteloot, Frédéric ; ; et alPoster (2009, May 24) Introduction. Recent data showed that subchondral bone plays an important role in osteoarthritis (OA). Metabolic and morphologic modifications in this tissue contribute to the degradation of the ... [more ▼] Introduction. Recent data showed that subchondral bone plays an important role in osteoarthritis (OA). Metabolic and morphologic modifications in this tissue contribute to the degradation of the overlaying cartilage. It was suggested that abnormal mechanical pressure exerted onto the articulation was responsible to these changes. Here, we evaluated the effects of compression on osteoblasts from subchondral bone. Method. Osteoblasts were isolated from sclerotic (SC) or non-sclerotic (NSC) areas of human OA subchondral bone. After 28 days, osteoblasts were surrounded by their matrix. This osteoblasts-containing membrane was then placed onto a Biopress Flexercell plate and submitted to a 4h 1.67 MPa compression (1 Hz). Expression of IL-6, IL-8, COX-2, VEGF, IGF-1, OPG and RANKL was evaluated by RT-PCR. IL-6, IL-8 and PGE2 were quantified by ELISA. Results. Basal IL-6, VEGF, COX-2, IGF-1 and RANKL mRNA levels were significantly increased in SC osteoblasts as compared to NSC. By contrast, SC osteoblasts expressed less OPG than those from NSC areas. Compressions induced the expression of genes coding for IL-6, IL-8, COX-2, IGF-1, VEGF and RANKL but decreased the expression of OPG in NSC osteoblasts (p<0.01). Interestingly, compressed NSC osteoblasts expressed similar levels of these genes than SC osteoblasts. Conclusions. We show that our model of compression can induce in NSC osteoblasts a phenotype similar to this observed in sclerotic areas. Moreover, SC osteoblasts are less sensitive to mechanical stimuli than NSC osteoblasts. These results clarify the role of compression in the pathogenesis of subchondral bone sclerosis and allow new perspectives of research in this field. [less ▲] Detailed reference viewed: 54 (1 ULg) Compression induces the expression of a sclerotic phenotype in human subchondral osteoblastsSanchez, Christelle ; ; Pesesse, Laurence et alPoster (2009) Detailed reference viewed: 15 (2 ULg) Compression induces the expression of a sclerotic phenotype in human subchondral osteoblastsSanchez, Christelle ; ; Pesesse, Laurence et alin Osteoarthritis and Cartilage (2009), 17(suppl 1), 95 Detailed reference viewed: 18 (2 ULg) Etude des effets de la compression sur le métabolisme des ostéoblastes sous-chondraux humainsSanchez, Christelle ; Mathy, Marianne ; et alPoster (2008) Detailed reference viewed: 4 (0 ULg) Study of the in vitro conditions promoting hypertrophic differentiation of osteoarthritic articular chondrocytesSanchez, Christelle ; Deberg, Michelle ; et alPoster (2008) Detailed reference viewed: 15 (3 ULg) Etude des effets de la compression sur le métabolisme des ostéoblastes sous-chondraux humainsSanchez, Christelle ; Mathy, Marianne ; et alin Revue du Rhumatisme (2008), 75(10-11), 1021 Detailed reference viewed: 10 (1 ULg) |
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