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Expression of 5-lipoxygenase and 15-lipoxygenase in rheumatoid arthritis synovium and effects of intraarticular glucocorticoids

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ARTHRITIS RESEARCH & THERAPY
卷 11, 期 3, 页码 -

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BIOMED CENTRAL LTD
DOI: 10.1186/ar2717

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  1. Karolinska Institutet
  2. Swedish Research Council
  3. The Swedish County Council
  4. The Swedish Rheumatism Association
  5. The Swedish Medical Society
  6. King Gustaf V 80-year fund

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Introduction It was previously shown that lipoxygenase (LO) pathways are important in the rheumatoid arthritis ( RA) inflammatory process and that synovial fluid from RA patients contains high amounts of leukotrienes. We therefore aimed to investigate the 5-LO and 15-LO-1 expression pattern in RA and ostheoarthritis (OA) synovial tissue and to study the effect of intraarticular glucocorticoid ( GC) therapy on enzyme expression. Methods Expression of LOs was evaluated by immunohistochemistry in RA and OA synovial biopsies. Cellular localization of these enzymes was analyzed by double immunofluorescence. In synovial biopsies from 11 RA patients, 5-LO and 15-LO-1 expression was evaluated before and after triamcinolone hexacetonide knee injection and assessed by image analysis to quantify their expression. We also investigated the presence of 15-LO-1 by immunohistochemistry in synovial fluid ( SF) cells as well as their ability to form 15- hydroxyeicosatetraenoic acid ( 15- HETE) following treatment with arachidonic acid (AA). Results 5-LO and 15-LO-1 are present in RA and OA synovium, with 5-LO being mostly expressed in lining and sublining macrophages, neutrophils and mast cells and 15-LO-1 mainly in lining macrophages, fibroblasts and sublining endothelial cells. Intraarticular GC treatment resulted in a significant suppression of 5-LO expression, but did not influence the 15-LO-1 enzyme significantly. Also, SF cells express a functional 15-LO-1 and produce 15- HETE when challenged with AA. Conclusions These data demonstrate that local therapy with GC decreases 5-LO expression in RA synovium and offer an additional possible mechanism for the efficiency of intraarticular adjuvant therapy in RA.

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