Department of Pathology, University of Cambridge, Cambridge, United Kingdom.
J Clin Invest. 2011 Sep;121(9):3505-16. doi: 10.1172/JCI45913. Epub 2011 Aug 15.
Osteoclasts are terminally differentiated leukocytes that erode the mineralized bone matrix. Osteoclastogenesis requires costimulatory receptor signaling through adaptors containing immunoreceptor tyrosine-based activation motifs (ITAMs), such as Fc receptor common γ (FcRγ) and DNAX-activating protein of 12 kDa. Identification of these ITAM-containing receptors and their ligands remains a high research priority, since the stimuli for osteoclastogenesis are only partly defined. Osteoclast-associated receptor (OSCAR) was proposed to be a potent FcRγ-associated costimulatory receptor expressed by preosteoclasts in vitro, but OSCAR lacks a cognate ligand and its role in vivo has been unclear. Using samples from mice and patients deficient in various ITAM signaling pathways, we show here that OSCAR costimulates one of the major FcRγ-associated pathways required for osteoclastogenesis in vivo. Furthermore, we found that OSCAR binds to specific motifs within fibrillar collagens in the ECM that become revealed on nonquiescent bone surfaces in which osteoclasts undergo maturation and terminal differentiation in vivo. OSCAR promoted osteoclastogenesis in vivo, and OSCAR binding to its collagen motif led to signaling that increased numbers of osteoclasts in culture. Thus, our results suggest that ITAM-containing receptors can respond to exposed ligands in collagen, leading to the functional differentiation of leukocytes, which provides what we believe to be a new concept for ITAM regulation of cytokine receptors in different tissue microenvironments.
破骨细胞是终末分化的白细胞,可侵蚀矿化的骨基质。破骨细胞生成需要共刺激受体信号通过包含免疫受体酪氨酸激活基序(ITAMs)的衔接子,例如 Fc 受体共同γ(FcRγ)和 12 kDa 的 DNAX 激活蛋白。这些含有 ITAM 的受体及其配体的鉴定仍然是一个高度研究的重点,因为破骨细胞生成的刺激因素仅部分定义。骨吸收相关受体(OSCAR)被提出是体外破骨前体细胞中表达的一种有效的 FcRγ 相关共刺激受体,但 OSCAR 缺乏同源配体,其在体内的作用尚不清楚。使用来自缺乏各种 ITAM 信号通路的小鼠和患者的样本,我们在这里表明 OSCAR 共刺激体内破骨细胞生成所需的主要 FcRγ 相关途径之一。此外,我们发现 OSCAR 结合到细胞外基质中纤维胶原内的特定基序,这些基序在非静止骨表面上显现,骨细胞在体内经历成熟和终末分化。OSCAR 在体内促进破骨细胞生成,OSCAR 与其胶原基序的结合导致信号增加培养物中破骨细胞的数量。因此,我们的结果表明,ITAM 包含的受体可以响应胶原中暴露的配体,导致白细胞的功能分化,这为我们认为是不同组织微环境中 ITAM 调节细胞因子受体的新概念提供了依据。