Department of Medicine, Division of Immunology and Rheumatology, Stanford University School of Medicine, CCSR 4135, 269 Campus Drive, Stanford, CA 94305, USA.
Arthritis Res Ther. 2010;12(1):R32. doi: 10.1186/ar2940. Epub 2010 Feb 24.
Tyrosine kinases are key mediators of multiple signaling pathways implicated in rheumatoid arthritis (RA). We previously demonstrated that imatinib mesylate--a Food and Drug Administration (FDA)-approved, antineoplastic drug that potently inhibits the tyrosine kinases Abl, c-Kit, platelet-derived growth factor receptor (PDGFR), and c-Fms--ameliorates murine autoimmune arthritis. However, which of the imatinib-targeted kinases is the principal culprit in disease pathogenesis remains unknown. Here we examine the role of c-Fms in autoimmune arthritis.
We tested the therapeutic efficacy of orally administered imatinib or GW2580, a small molecule that specifically inhibits c-Fms, in three mouse models of RA: collagen-induced arthritis (CIA), anti-collagen antibody-induced arthritis (CAIA), and K/BxN serum transfer-induced arthritis (K/BxN). Efficacy was evaluated by visual scoring of arthritis severity, paw thickness measurements, and histological analysis. We assessed the in vivo effects of imatinib and GW2580 on macrophage infiltration of synovial joints in CIA, and their in vitro effects on macrophage and osteoclast differentiation, and on osteoclast-mediated bone resorption. Further, we determined the effects of imatinib and GW2580 on the ability of macrophage colony-stimulating factor (M-CSF; the ligand for c-Fms) to prime bone marrow-derived macrophages to produce tumor necrosis factor (TNF) upon subsequent Fc receptor ligation. Finally, we measured M-CSF levels in synovial fluid from patients with RA, osteoarthritis (OA), or psoriatic arthritis (PsA), and levels of total and phosphorylated c-Fms in synovial tissue from patients with RA.
GW2580 was as efficacious as imatinib in reducing arthritis severity in CIA, CAIA, and K/BxN models of RA. Specific inhibition of c-Fms abrogated (i) infiltration of macrophages into synovial joints of arthritic mice; (ii) differentiation of monocytes into macrophages and osteoclasts; (iii) osteoclast-mediated bone resorption; and (iv) priming of macrophages to produce TNF upon Fc receptor stimulation, an important trigger of synovitis in RA. Expression and activation of c-Fms in RA synovium were high, and levels of M-CSF were higher in RA synovial fluid than in OA or PsA synovial fluid.
These results suggest that c-Fms plays a central role in the pathogenesis of RA by mediating the differentiation and priming of monocyte lineage cells. Therapeutic targeting of c-Fms could provide benefit in RA.
酪氨酸激酶是多种信号通路的关键介质,这些信号通路与类风湿关节炎(RA)有关。我们之前证明甲磺酸伊马替尼——一种美国食品和药物管理局(FDA)批准的抗肿瘤药物,能强力抑制酪氨酸激酶 Abl、c-Kit、血小板衍生生长因子受体(PDGFR)和 c-Fms——可改善小鼠自身免疫性关节炎。然而,伊马替尼靶向的激酶中哪一种是疾病发病机制中的主要罪魁祸首尚不清楚。在这里,我们研究了 c-Fms 在自身免疫性关节炎中的作用。
我们在三种 RA 小鼠模型中测试了口服给予伊马替尼或 GW2580(一种特异性抑制 c-Fms 的小分子)的治疗效果:胶原诱导性关节炎(CIA)、抗胶原抗体诱导性关节炎(CAIA)和 K/BxN 血清转移诱导性关节炎(K/BxN)。通过关节炎严重程度的视觉评分、爪厚度测量和组织学分析来评估疗效。我们评估了伊马替尼和 GW2580 对 CIA 中滑膜关节巨噬细胞浸润的体内影响,以及它们对巨噬细胞和破骨细胞分化以及破骨细胞介导的骨吸收的体外影响。此外,我们确定了伊马替尼和 GW2580 对巨噬细胞集落刺激因子(M-CSF;c-Fms 的配体)的能力的影响,即在随后的 Fc 受体交联时,M-CSF 可使骨髓来源的巨噬细胞产生肿瘤坏死因子(TNF)。最后,我们测量了 RA、骨关节炎(OA)或银屑病关节炎(PsA)患者滑液中的 M-CSF 水平,以及 RA 患者滑膜组织中的总 c-Fms 和磷酸化 c-Fms 水平。
GW2580 在 CIA、CAIA 和 K/BxN 模型中减轻关节炎严重程度的效果与伊马替尼一样有效。c-Fms 的特异性抑制(i)阻断了关节炎小鼠滑膜关节中巨噬细胞的浸润;(ii)单核细胞向巨噬细胞和破骨细胞的分化;(iii)破骨细胞介导的骨吸收;以及(iv)Fc 受体刺激时巨噬细胞产生 TNF 的预刺激,这是 RA 滑膜炎症的重要触发因素。RA 滑膜中 c-Fms 的表达和激活水平较高,RA 滑液中的 M-CSF 水平高于 OA 或 PsA 滑液。
这些结果表明,c-Fms 通过介导单核细胞系细胞的分化和预刺激,在 RA 的发病机制中发挥核心作用。针对 c-Fms 的治疗性靶向可能对 RA 有益。