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本文引用的文献

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Receptor becomes a ligand to control bone remodelling.受体成为控制骨重塑的配体。
Nature. 2018 Sep;561(7722):180-181. doi: 10.1038/d41586-018-05960-x.
2
Coupling of bone resorption and formation by RANKL reverse signalling.RANKL 反向信号转导耦联骨吸收与形成。
Nature. 2018 Sep;561(7722):195-200. doi: 10.1038/s41586-018-0482-7. Epub 2018 Sep 5.
3
High Plasma Sphingosine 1-phosphate Levels Predict Osteoporotic Fractures in Postmenopausal Women: The Center of Excellence for Osteoporosis Research Study.高血浆鞘氨醇-1-磷酸水平可预测绝经后女性骨质疏松性骨折:骨质疏松症卓越研究中心研究
J Bone Metab. 2018 May;25(2):87-98. doi: 10.11005/jbm.2018.25.2.87. Epub 2018 May 31.
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Understanding axon guidance: are we nearly there yet?了解轴突导向:我们快成功了吗?
Development. 2018 May 14;145(10):dev151415. doi: 10.1242/dev.151415.
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WAIF1 Is a Cell-Surface CTHRC1 Binding Protein Coupling Bone Resorption and Formation.WAIF1 是一种细胞表面 CTHRC1 结合蛋白,耦联骨吸收与形成。
J Bone Miner Res. 2018 Aug;33(8):1500-1512. doi: 10.1002/jbmr.3436. Epub 2018 May 11.
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Opening windows for bone remodeling through a SLIT.通过 SLIT 打开骨骼重塑的窗口。
J Clin Invest. 2018 Apr 2;128(4):1255-1257. doi: 10.1172/JCI120325. Epub 2018 Mar 5.
7
Osteoclast-secreted SLIT3 coordinates bone resorption and formation.破骨细胞分泌的 SLIT3 协调骨吸收和形成。
J Clin Invest. 2018 Apr 2;128(4):1429-1441. doi: 10.1172/JCI91086. Epub 2018 Mar 5.
8
Direct cell-cell contact between mature osteoblasts and osteoclasts dynamically controls their functions in vivo.成熟成骨细胞与破骨细胞之间的直接细胞间接触在体内动态控制它们的功能。
Nat Commun. 2018 Jan 19;9(1):300. doi: 10.1038/s41467-017-02541-w.
9
Coupling factors and exosomal packaging microRNAs involved in the regulation of bone remodelling.参与骨重建调节的偶联因子和外泌体包装 microRNAs。
Biol Rev Camb Philos Soc. 2018 Feb;93(1):469-480. doi: 10.1111/brv.12353. Epub 2017 Aug 10.
10
Cathepsin K Inhibitors for Osteoporosis: Biology, Potential Clinical Utility, and Lessons Learned.组织蛋白酶 K 抑制剂治疗骨质疏松症:生物学、潜在临床应用及经验教训。
Endocr Rev. 2017 Aug 1;38(4):325-350. doi: 10.1210/er.2015-1114.

涉及维持骨平衡的偶联因子。

Coupling factors involved in preserving bone balance.

机构信息

Division of Endocrinology and Metabolism, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, South Korea.

出版信息

Cell Mol Life Sci. 2019 Apr;76(7):1243-1253. doi: 10.1007/s00018-018-2981-y. Epub 2018 Dec 4.

DOI:10.1007/s00018-018-2981-y
PMID:30515522
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11105749/
Abstract

Coupling during bone remodeling refers to the spatial and temporal coordination of bone resorption with bone formation. Studies have assessed the subtle interactions between osteoclasts and osteoblasts to preserve bone balance. Traditionally, coupling research related to osteoclast function has focused on bone resorption activity causing the release of growth factors embedded in the bone matrix. However, considerable evidence from in vitro, animal, and human studies indicates the importance of the osteoclasts themselves in coupling phenomena, and many osteoclast-derived coupling factors have been identified. These include sphingosine-1-phosphate, vesicular-receptor activator of nuclear factor-κB, collagen triple helix repeat containing 1, and cardiotrophin-1. Interestingly, neuronal guidance molecules, such as slit guidance ligand 3, semaphorin (SEMA) 3A, SEMA4D, and netrin-1, originally identified as instructive cues allowing the navigation of growing axons to their targets, have been shown to be involved in the intercellular cross-talk among bone cells. This review discusses osteoclast-osteoblast coupling signals, including recent advances and the potential roles of these signals as therapeutic targets for osteoporosis and as biomarkers predicting human bone health.

摘要

骨重建过程中的偶联是指骨吸收与骨形成在时空上的协调。研究评估了破骨细胞和成骨细胞之间的微妙相互作用,以维持骨平衡。传统上,与破骨细胞功能相关的偶联研究集中在骨吸收活动上,该活动导致嵌入骨基质中的生长因子的释放。然而,来自体外、动物和人体研究的大量证据表明破骨细胞本身在偶联现象中的重要性,并且已经鉴定出许多破骨细胞衍生的偶联因子。这些包括鞘氨醇-1-磷酸、囊泡受体激活核因子-κB、胶原三螺旋重复序列 1 和心肌营养素-1。有趣的是,最初被认为是指导生长轴突向其靶标导航的指令性线索的神经元导向分子,如缝隙连接配体 3、神经鞘氨醇 (SEMA) 3A、SEMA4D 和 netrin-1,已被证明参与骨细胞之间的细胞间串扰。这篇综述讨论了破骨细胞-成骨细胞偶联信号,包括这些信号的最新进展及其作为骨质疏松症治疗靶点和预测人类骨骼健康的生物标志物的潜在作用。