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本文引用的文献

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Biology of Bone Tissue: Structure, Function, and Factors That Influence Bone Cells.骨组织生物学:结构、功能及影响骨细胞的因素
Biomed Res Int. 2015;2015:421746. doi: 10.1155/2015/421746. Epub 2015 Jul 13.
2
MicroRNAs in Bone Balance and Osteoporosis.骨平衡与骨质疏松症中的微小RNA
Drug Dev Res. 2015 Aug;76(5):235-45. doi: 10.1002/ddr.21260. Epub 2015 Jul 27.
3
Combined effect of bisphosphonate and recombinant human bone morphogenetic protein 2 on bone healing of rat calvarial defects.双膦酸盐与重组人骨形态发生蛋白2对大鼠颅骨缺损骨愈合的联合作用
Maxillofac Plast Reconstr Surg. 2015 Jul 2;37(1):16. doi: 10.1186/s40902-015-0015-3. eCollection 2015 Dec.
4
Studies of OC-STAMP in Osteoclast Fusion: A New Knockout Mouse Model, Rescue of Cell Fusion, and Transmembrane Topology.破骨细胞融合中OC-STAMP的研究:一种新的基因敲除小鼠模型、细胞融合的挽救及跨膜拓扑结构
PLoS One. 2015 Jun 4;10(6):e0128275. doi: 10.1371/journal.pone.0128275. eCollection 2015.
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Acceleration of callus formation during fracture healing using basic fibroblast growth factor-kidney disease domain-collagen-binding domain fusion protein combined with allogenic demineralized bone powder.使用碱性成纤维细胞生长因子-肾病结构域-胶原结合结构域融合蛋白联合同种异体脱矿骨粉加速骨折愈合过程中骨痂的形成。
J Orthop Surg Res. 2015 May 9;10:59. doi: 10.1186/s13018-015-0201-0.
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Loss of Gi G-Protein-Coupled Receptor Signaling in Osteoblasts Accelerates Bone Fracture Healing.成骨细胞中Gi G蛋白偶联受体信号的丧失加速骨折愈合。
J Bone Miner Res. 2015 Oct;30(10):1896-904. doi: 10.1002/jbmr.2540. Epub 2015 May 14.
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Mechanical microenvironments and protein expression associated with formation of different skeletal tissues during bone healing.与骨愈合过程中不同骨骼组织形成相关的机械微环境和蛋白质表达。
Biomech Model Mechanobiol. 2015 Nov;14(6):1239-53. doi: 10.1007/s10237-015-0670-4. Epub 2015 Mar 31.
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Polyhedral microcrystals encapsulating bone morphogenetic protein 2 improve healing in the alveolar ridge.包裹骨形态发生蛋白2的多面体微晶可促进牙槽嵴愈合。
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Osteoblast-induced osteoclast apoptosis by fas ligand/FAS pathway is required for maintenance of bone mass.成骨细胞通过Fas配体/FAS途径诱导破骨细胞凋亡是维持骨量所必需的。
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DC-STAMP:破骨细胞分化中的关键调节因子。

DC-STAMP: A Key Regulator in Osteoclast Differentiation.

作者信息

Chiu Ya-Hui, Ritchlin Christopher T

机构信息

Division of Allergy, Immunology and Rheumatology, School of Medicine, University of Rochester, Rochester, New York.

出版信息

J Cell Physiol. 2016 Nov;231(11):2402-7. doi: 10.1002/jcp.25389. Epub 2016 Jun 14.

DOI:10.1002/jcp.25389
PMID:27018136
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4946985/
Abstract

Osteoimmunology research is a new emerging research field that investigates the links between the bone and immune responses. Results from osteoimmunology studies suggest that bone is not only an essential component of the musculoskeletal system, but is also actively involved in immune regulation. Many important factors involved in immune regulation also participate in bone homeostasis. Bone homeostasis is achieved by a coordinated action between bone-synthesizing osteoblasts and bone-degrading osteoclasts. An imbalanced action between osteoblasts and osteoclasts often results in pathological bone diseases: osteoporosis is caused by an excessive osteoclast activity, whereas osteopetrosis results from an increased osteoblast activity. This review focuses on dendritic cell-specific transmembrane protein (DC-STAMP), an important protein currently considered as a master regulator of osteoclastogenesis. Of clinical relevance, the frequency of circulating DC-STAMP+ cells is elevated during the pathogenesis of psoriatic diseases. Intriguingly, recent results suggest that DC-STAMP also plays an imperative role in bone homeostasis by regulating the differentiation of both osteoclasts and osteoblasts. This article summarizes our current knowledge on DC-STAMP by focusing on its interacting proteins, its regulation on osteoclastogenesis-related genes, its possible involvement in immunoreceptor tyrosine-based inhibitory motif (ITIM)-mediated signaling cascade, and its potential of developing therapeutics for clinical applications. J. Cell. Physiol. 231: 2402-2407, 2016. © 2016 Wiley Periodicals, Inc.

摘要

骨免疫学研究是一个新兴的研究领域,旨在探究骨骼与免疫反应之间的联系。骨免疫学研究结果表明,骨骼不仅是肌肉骨骼系统的重要组成部分,还积极参与免疫调节。许多参与免疫调节的重要因子也参与骨稳态的维持。骨稳态是由成骨细胞合成骨和破骨细胞降解骨的协调作用实现的。成骨细胞和破骨细胞之间的作用失衡通常会导致病理性骨疾病:骨质疏松症是由破骨细胞活性过高引起的,而骨质石化则是由成骨细胞活性增加导致的。本综述聚焦于树突状细胞特异性跨膜蛋白(DC-STAMP),这是一种目前被认为是破骨细胞生成主要调节因子的重要蛋白。具有临床相关性的是,在银屑病发病过程中,循环DC-STAMP+细胞的频率会升高。有趣的是,最近的研究结果表明,DC-STAMP还通过调节破骨细胞和成骨细胞的分化在骨稳态中发挥重要作用。本文通过聚焦其相互作用蛋白、对破骨细胞生成相关基因的调节、可能参与基于免疫受体酪氨酸的抑制基序(ITIM)介导的信号级联反应以及其开发临床应用治疗方法的潜力,总结了我们目前对DC-STAMP的认识。《细胞生理学杂志》231: 2402 - 2407, 2016年。© 2016威利期刊公司。