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    Bone. 2004 Aug;35(2):463-70.

    Expression of ICAM-1 by osteoblasts in healthy individuals and in patients suffering from osteoarthritis and osteoporosis.

    Lavigne P, Benderdour M, Lajeunesse D, Shi Q, Fernandes JC.

    Orthopaedics Research Laboratory, Department of Orthopaedics, Centre hospitalier Sacré-Coeur, Montreal, Quebec, Canada.

    OBJECTIVES: To describe the pattern of expression of intercellular adhesion molecule-1 (ICAM-1) at the surface of human osteoblasts (Ob) recovered from normal (control), osteoporotic (OP), and osteoarthritic (OA) bone. To relate ICAM-1 expression in OA Ob with interleukin-6 (IL-6) and prostaglandin E2 (PGE2) production. MATERIALS AND METHODS: Trabecular bone specimens were taken from patients suffering from OA of the hip (n = 19) or knee (n = 19) or from hip fracture caused by osteoporosis (n = 10). Control bone specimens came from the posterosuperior iliac crest (n = 5) and from the femoral condyle of organ donors (n = 6). Bone explants were digested with collagenase and cultured. Ob were obtained after 6 weeks. ICAM-1 expression was studied by immunocytology. IL-6 and PGE2 were evaluated by standard ELISA. RESULTS: Average ICAM-1 expression was different between control and OP bone (P < 0.02). Separation of specimens into high and low ICAM-1 expression showed a significant difference between high and low ICAM-1 expressors. The distribution of specimens after subclassification into high or low ICAM-1 expression groups revealed only 18.2% of patients in the high expression group for the controls, compared to 70% for OP bone (P < 0.03), 52.6% for hip OA and 47.4% for knee OA. IL-6 and PGE2 levels in OA Ob from both groups were found to be significantly elevated with high ICAM-1 expression compared to low ICAM-1 expression. CONCLUSION: The results show that ICAM-1 expression in human bone seems to be pathology-dependent and correlates with IL-6 and PGE2 production, at least in OA individuals. This implies that ICAM-1 could discriminate functionally different populations of Ob and possibly alter the clinical evolution of the disease.

    PMID: 15268898 [PubMed - indexed for MEDLINE]

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