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本文引用的文献

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Paired immunoglobin-like receptor-B regulates the suppressive function and fate of myeloid-derived suppressor cells.配对免疫球蛋白样受体-B 调节髓源性抑制细胞的抑制功能和命运。
Immunity. 2011 Mar 25;34(3):385-95. doi: 10.1016/j.immuni.2011.02.004. Epub 2011 Mar 3.
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Alternative activation of macrophages: mechanism and functions.巨噬细胞的替代激活:机制与功能。
Immunity. 2010 May 28;32(5):593-604. doi: 10.1016/j.immuni.2010.05.007.
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TREM2- and DAP12-dependent activation of PI3K requires DAP10 and is inhibited by SHIP1.TREM2 和 DAP12 依赖性的 PI3K 激活需要 DAP10,并被 SHIP1 抑制。
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Development of monocytes, macrophages, and dendritic cells.单核细胞、巨噬细胞和树突状细胞的发育。
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Matrix crosslinking forces tumor progression by enhancing integrin signaling.基质交联通过增强整合素信号传导促进肿瘤进展。
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Ca2+-NFATc1 signaling is an essential axis of osteoclast differentiation.钙离子-NFATc1信号传导是破骨细胞分化的关键轴。
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Inhibitory regulation of osteoclast bone resorption by signal regulatory protein alpha.信号调节蛋白 α对破骨细胞骨吸收的抑制调节。
FASEB J. 2009 Dec;23(12):4081-90. doi: 10.1096/fj.09-131557. Epub 2009 Aug 10.
8
Macrophage colony-stimulating factor induces the proliferation and survival of macrophages via a pathway involving DAP12 and beta-catenin.巨噬细胞集落刺激因子通过一条涉及DAP12和β-连环蛋白的信号通路诱导巨噬细胞的增殖和存活。
Nat Immunol. 2009 Jul;10(7):734-43. doi: 10.1038/ni.1744. Epub 2009 Jun 7.
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Cross-regulation of signaling by ITAM-associated receptors.ITAM 相关受体对信号的交叉调节。
Nat Immunol. 2009 Apr;10(4):340-7. doi: 10.1038/ni.1706. Epub 2009 Mar 19.
10
Bone marrow monocyte PECAM-1 deficiency elicits increased osteoclastogenesis resulting in trabecular bone loss.骨髓单核细胞PECAM-1缺乏会引发破骨细胞生成增加,导致小梁骨丢失。
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OSCAR 是一种胶原蛋白受体,可在 DAP12 缺陷的人类和小鼠中增强破骨细胞生成。

OSCAR is a collagen receptor that costimulates osteoclastogenesis in DAP12-deficient humans and mice.

机构信息

Department of Pathology, University of Cambridge, Cambridge, United Kingdom.

出版信息

J Clin Invest. 2011 Sep;121(9):3505-16. doi: 10.1172/JCI45913. Epub 2011 Aug 15.

DOI:10.1172/JCI45913
PMID:21841309
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3163954/
Abstract

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.

摘要

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。