Enhanced osteoclastogenesis in patients with tophaceous gout: Urate crystals promote osteoclast development through interactions with stromal cells

破骨细胞 兰克尔 外周血单个核细胞 痛风 间质细胞 多核 化学 抗酒石酸酸性磷酸酶 病理 医学 癌症研究 分子生物学 免疫学 内科学 生物 体外 生物化学 受体 激活剂(遗传学)
作者
Nicola Dalbeth,Timothy W. Smith,Bridget Nicolson,Barnaby Clark,Karen E. Callon,Dorit Naot,Dorian O. Haskard,Fiona McQueen,Ian R. Reid,Jillian Cornish
出处
期刊:Arthritis & Rheumatism [Wiley]
卷期号:58 (6): 1854-1865 被引量:145
标识
DOI:10.1002/art.23488
摘要

Abstract Objective To analyze cellular mechanisms of bone erosion in gout. Methods Peripheral blood mononuclear cells (PBMCs) and synovial fluid mononuclear cells (SFMCs) from patients with gout were analyzed for the presence of osteoclast precursors. Fixed tophus and bone samples were analyzed by immunohistochemistry. Mechanisms of osteoclastogenesis were studied by culturing murine preosteoclast RAW 264.7 cells, bone marrow stromal ST2 cells, and human synovial fibroblasts with monosodium urate monohydrate (MSU) crystals. Results PBMCs from patients with severe erosive gout had the preferential ability to form osteoclast‐like cells in culture with RANKL and monocyte colony‐stimulating factor (M‐CSF). The number of PBMC‐derived tartrate‐resistant acid phosphatase (TRAP)–positive multinucleated cells strongly correlated with the number of tophi (r = 0.6296, P = 0.630). Patients with severe erosive and tophaceous gout also had higher circulating concentrations of RANKL and M‐CSF. Furthermore, greater numbers of TRAP‐positive multinucleated cells were cultured from SFMCs derived from gouty knee effusions than from paired PBMCs ( P = 0.004). Immunohistochemical analysis demonstrated numerous multinucleated cells expressing osteoclast markers within tophi and at the interface between soft tissue and bone. MSU crystals did not directly promote osteoclast formation from RAW 264.7 cells in vitro. However, MSU crystals inhibited osteoprotegerin gene and protein expression in ST2 cells and human synovial fibroblasts, without significantly altering RANKL gene expression. Conditioned medium from ST2 cells cultured with MSU crystals promoted osteoclast formation from RAW 264.7 cells in the presence of RANKL. Conclusion Chronic tophaceous and erosive gout is characterized by enhanced osteoclast development. These data provide a rationale for the study of osteoclast‐targeted therapies for the prevention of bone damage in chronic gout.
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