首页> 外文期刊>Clinica chimica acta: International journal of clinical chemistry and applied molecular biology >Dipeptidyl peptidase-IV in synovial fluid and in synovial fluid mononuclear cells of patients with rheumatoid arthritis.
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Dipeptidyl peptidase-IV in synovial fluid and in synovial fluid mononuclear cells of patients with rheumatoid arthritis.

机译:双肽肽酶 - IV在滑液中和类风湿性关节炎患者的滑膜异核细胞。

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摘要

BACKGROUND: Dipeptidyl peptidase-IV (DPP-IV) enzymatic activity controls biological halftime of multiple local mediators. Its deregulation is associated with pathogenesis of several autoimmune diseases, including rheumatoid arthritis (RA). Although DPP-IV is the canonical representative of the group, a number of other proteins have been shown to have similar enzymatic activity. This study was aimed to identify the molecular source of DPP-IV activity in synovial fluid (SF) and fluid mononuclear cells (FMNC) in patients with RA and osteoarthritis (OA). In addition, the association of DPP-IV and the concentration of stromal cell-derived factor-1alpha (SDF), DPP-IV substrate, were evaluated. METHODS: DPP-IV activity was measured by the kinetic fluorimetric method. The expression of studied molecules in FMNC and their concentrations in SF were assayed using flow cytometry and ELISA respectively. RESULTS: DPP-IV activity in SF, dominantly derived from the canonical DPP-IV, does not significantly differ between RA and OA. However, a significantly lower DPP-IV activity and expression in FMNC was found in RA as opposed to OA patients. Negative correlation between SDF concentration in SF and the relative amount of CD3+CD26+ cells was observed. CONCLUSIONS: We report decreased presence of DPP-IV/CD26 in CD3+ FMNC in RA, which also may participate on impaired balance of SDF concentration in SF.
机译:背景:二肽肽酶-4- in酶(DPP-IV)酶活性控制多个局部介质的生物学半场。其放松管制与几种自身免疫疾病的发病机制有关,包括类风湿性关节炎(RA)。虽然DPP-IV是该组的规范代表,但已经显示了许多其他蛋白质具有相似的酶活性。该研究旨在鉴定RA和骨关节炎(OA)中的滑膜液(SF)和流体单核细胞(FMNC)中DPP-IV活性的分子源。另外,评价DPP-IV的关联和基质细胞衍生因子-1Alpha(SDF),DPP-IV衬底的浓度。方法:通过动力学荧光法测量DPP-IV活性。使用流式细胞术和ELISA测定研究FMNC中研究分子及其在SF中的浓度。结果:SF中的DPP-IV活性,源自广义DPP-IV,RA和OA之间的显着不同。然而,在RA中发现了对FMNC的显着降低的DPP-IV活性和表达,而不是OA患者。观察到SFF浓度与CD3 + CD26 +细胞的相对量之间的负相关。结论:我们报告了RA中CD3 + FMNC中DPP-IV / CD26的存在下降,这也可参与SF中的SDF浓度的受损平衡。

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