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单核细胞中的OSCAR-胶原蛋白信号传导发挥促炎作用,并可能促成类风湿性关节炎的发病机制。

OSCAR-collagen signaling in monocytes plays a proinflammatory role and may contribute to the pathogenesis of rheumatoid arthritis.

作者信息

Schultz Heidi S, Guo Li, Keller Pernille, Fleetwood Andrew J, Sun Mingyi, Guo Wei, Ma Chunyan, Hamilton John A, Bjørkdahl Olle, Berchtold Martin W, Panina Svetlana

机构信息

Biopharmaceutical Research Unit, Novo Nordisk A/S, Måløv, Denmark.

Department of Biology, Copenhagen University, Copenhagen, Denmark.

出版信息

Eur J Immunol. 2016 Apr;46(4):952-63. doi: 10.1002/eji.201545986. Epub 2016 Feb 9.

Abstract

Osteoclast-associated receptor (OSCAR) is an activating receptor expressed by human myeloid cells. Collagen type I (ColI) and collagen type II (ColII) serve as ligands for OSCAR. OSCAR-collagen interaction stimulates RANK-dependent osteoclastogenesis. We have recently reported that OSCAR promotes functional maturation of monocyte-derived dendritic cells. OSCAR is upregulated on monocytes from rheumatoid arthritis (RA) patients with active disease, and these monocytes show an increased proosteoclastogenic potential. In the current study, we have addressed a functional role for an OSCAR-collagen interaction on monocytes. We show that OSCAR-ColII signaling promoted the survival of monocytes. Moreover, ColII stimulated the release of proinflammatory cytokines by monocytes from healthy donors, which could be completely blocked by an anti-OSCAR monoclonal antibody. Mononuclear cells from the synovial fluid of RA patients plated on ColII secreted TNF-α and IL-8 in an OSCAR-dependent manner. Global RNA profiling showed that components of multiple signaling pathways relevant to RA pathogenesis are regulated at the transcriptional level by OSCAR in monocytes. Thus, OSCAR can play a proinflammatory role in monocyte-derived cells and may contribute crucially on multiple levels to RA pathogenesis.

摘要

破骨细胞相关受体(OSCAR)是一种由人类髓系细胞表达的激活受体。I型胶原蛋白(ColI)和II型胶原蛋白(ColII)作为OSCAR的配体。OSCAR与胶原蛋白的相互作用刺激RANK依赖的破骨细胞生成。我们最近报道,OSCAR促进单核细胞衍生的树突状细胞的功能成熟。在患有活动性疾病的类风湿关节炎(RA)患者的单核细胞上,OSCAR表达上调,并且这些单核细胞显示出增加的促破骨细胞生成潜力。在当前的研究中,我们探讨了OSCAR与胶原蛋白相互作用对单核细胞的功能作用。我们发现OSCAR-ColII信号传导促进了单核细胞的存活。此外,ColII刺激健康供体的单核细胞释放促炎细胞因子,这可以被抗OSCAR单克隆抗体完全阻断。接种在ColII上的RA患者滑液中的单核细胞以OSCAR依赖的方式分泌TNF-α和IL-8。全基因组RNA分析表明,与RA发病机制相关的多个信号通路的成分在转录水平上受到单核细胞中OSCAR的调节。因此,OSCAR可以在单核细胞衍生的细胞中发挥促炎作用,并且可能在多个层面上对RA发病机制起关键作用。

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