• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

骨形态发生蛋白信号通路:破骨细胞视角

The Bone Morphogenetic Protein Pathway: The Osteoclastic Perspective.

作者信息

Lademann Franziska, Hofbauer Lorenz C, Rauner Martina

机构信息

Department of Medicine III, Technische Universität Dresden, Dresden, Germany.

Center for Healthy Aging, Technische Universität Dresden, Dresden, Germany.

出版信息

Front Cell Dev Biol. 2020 Oct 16;8:586031. doi: 10.3389/fcell.2020.586031. eCollection 2020.

DOI:10.3389/fcell.2020.586031
PMID:33178699
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7597383/
Abstract

Bone health crucially relies on constant bone remodeling and bone regeneration, both tightly controlled processes requiring bone formation and bone resorption. Plenty of evidence identifies bone morphogenetic proteins (BMP) as major players in osteoblast differentiation and thus, bone formation. However, in recent past years, researchers also increasingly reported on the pivotal role of these multi-functional growth factors in osteoclast formation and activity. This review aims to summarize the current knowledge of BMP signaling within the osteoclast lineage, its role in bone resorption, and osteoblast-osteoclast coupling. Furthermore, subsequent clinical implications for recombinant BMP therapy will be discussed in view of recent preclinical and clinical studies.

摘要

骨骼健康关键依赖于持续的骨重塑和骨再生,这两个过程都受到严格控制,需要骨形成和骨吸收。大量证据表明骨形态发生蛋白(BMP)是成骨细胞分化以及骨形成的主要参与者。然而,在过去几年中,研究人员也越来越多地报道了这些多功能生长因子在破骨细胞形成和活性中的关键作用。本综述旨在总结目前关于破骨细胞谱系中BMP信号传导的知识、其在骨吸收中的作用以及成骨细胞 - 破骨细胞偶联。此外,鉴于最近的临床前和临床研究,还将讨论重组BMP治疗的后续临床意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6091/7597383/347210311645/fcell-08-586031-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6091/7597383/347210311645/fcell-08-586031-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6091/7597383/347210311645/fcell-08-586031-g001.jpg

相似文献

1
The Bone Morphogenetic Protein Pathway: The Osteoclastic Perspective.骨形态发生蛋白信号通路:破骨细胞视角
Front Cell Dev Biol. 2020 Oct 16;8:586031. doi: 10.3389/fcell.2020.586031. eCollection 2020.
2
The Role Of BMPs in the Regulation of Osteoclasts Resorption and Bone Remodeling: From Experimental Models to Clinical Applications.BMPs 在破骨细胞吸收和骨重塑中的作用:从实验模型到临床应用。
Front Immunol. 2022 Apr 26;13:869422. doi: 10.3389/fimmu.2022.869422. eCollection 2022.
3
Direct stimulation of osteoclastic bone resorption by bone morphogenetic protein (BMP)-2 and expression of BMP receptors in mature osteoclasts.骨形态发生蛋白(BMP)-2对破骨细胞骨吸收的直接刺激作用以及BMP受体在成熟破骨细胞中的表达。
Bone. 2000 Oct;27(4):479-86. doi: 10.1016/s8756-3282(00)00358-6.
4
Bone morphogenetic proteins 5 and 6 stimulate osteoclast generation.骨形态发生蛋白5和6刺激破骨细胞生成。
J Biomed Mater Res A. 2006 Apr;77(1):75-83. doi: 10.1002/jbm.a.30615.
5
Controversy of physiological vs. pharmacological effects of BMP signaling: Constitutive activation of BMP type IA receptor-dependent signaling in osteoblast lineage enhances bone formation and resorption, not affecting net bone mass.骨形态发生蛋白(BMP)信号的生理与药理作用之争:成骨细胞系中 BMP Ⅰ型受体依赖性信号的组成性激活增强了骨形成和吸收,但不影响净骨量。
Bone. 2020 Sep;138:115513. doi: 10.1016/j.bone.2020.115513. Epub 2020 Jun 27.
6
Stimulatory effect of bone morphogenetic protein-2 on osteoclast-like cell formation and bone-resorbing activity.骨形态发生蛋白-2对破骨细胞样细胞形成和骨吸收活性的刺激作用。
J Bone Miner Res. 1995 Nov;10(11):1681-90. doi: 10.1002/jbmr.5650101110.
7
Regulation of bone formation by osteoclasts involves Wnt/BMP signaling and the chemokine sphingosine-1-phosphate.破骨细胞对骨形成的调节涉及Wnt/骨形态发生蛋白信号通路和趋化因子鞘氨醇-1-磷酸。
Proc Natl Acad Sci U S A. 2008 Dec 30;105(52):20764-9. doi: 10.1073/pnas.0805133106. Epub 2008 Dec 15.
8
Essential requirement of BMPs-2/4 for both osteoblast and osteoclast formation in murine bone marrow cultures from adult mice: antagonism by noggin.骨形态发生蛋白-2/4对成年小鼠骨髓培养中破骨细胞与成骨细胞形成的基本需求:诺金蛋白的拮抗作用
J Bone Miner Res. 2000 Apr;15(4):663-73. doi: 10.1359/jbmr.2000.15.4.663.
9
The Smad Dependent TGF-β and BMP Signaling Pathway in Bone Remodeling and Therapies.骨重塑与治疗中依赖Smad的TGF-β和BMP信号通路
Front Mol Biosci. 2021 May 5;8:593310. doi: 10.3389/fmolb.2021.593310. eCollection 2021.
10
Bone morphogenetic proteins in bone stimulate osteoclasts and osteoblasts during bone development.骨骼中的骨形态发生蛋白在骨骼发育过程中刺激破骨细胞和成骨细胞。
J Bone Miner Res. 2006 Jul;21(7):1022-33. doi: 10.1359/jbmr.060411.

引用本文的文献

1
Conotoxins from sea snails as potential bone remodeling disruptors.来自海螺的芋螺毒素作为潜在的骨重塑干扰物。
JBMR Plus. 2025 Feb 10;9(8):ziaf025. doi: 10.1093/jbmrpl/ziaf025. eCollection 2025 Aug.
2
Energy metabolism dysfunction and therapeutic strategies for treating temporomandibular disorders.颞下颌关节紊乱病的能量代谢功能障碍及治疗策略
Front Med (Lausanne). 2025 Jun 26;12:1581446. doi: 10.3389/fmed.2025.1581446. eCollection 2025.
3
Mechanisms of Ellagic Acid (EA)-Mediated Osteogenic Differentiation of Human Dental Pulp-Derived Stem Cells.

本文引用的文献

1
Disruption of BMP Signaling Prevents Hyperthyroidism-Induced Bone Loss in Male Mice.BMP 信号中断可预防男性小鼠甲亢性骨丢失。
J Bone Miner Res. 2020 Oct;35(10):2058-2069. doi: 10.1002/jbmr.4092. Epub 2020 Jun 15.
2
Bone Morphogenetic Protein 4 Gene Therapy in Mice Inhibits Myeloma Tumor Growth, But Has a Negative Impact on Bone.小鼠骨形态发生蛋白4基因治疗可抑制骨髓瘤肿瘤生长,但对骨骼有负面影响。
JBMR Plus. 2019 Nov 22;4(1):e10247. doi: 10.1002/jbm4.10247. eCollection 2020 Jan.
3
Erythromyeloid progenitors give rise to a population of osteoclasts that contribute to bone homeostasis and repair.
鞣花酸(EA)介导人牙髓来源干细胞成骨分化的机制
ACS Omega. 2025 Apr 13;10(15):15229-15242. doi: 10.1021/acsomega.4c10642. eCollection 2025 Apr 22.
4
Investigating the Influence of a Tooth Absence on Facial Bone Growth Using a Porcine Model.使用猪模型研究牙齿缺失对面部骨骼生长的影响。
Int J Mol Sci. 2024 Nov 21;25(23):12509. doi: 10.3390/ijms252312509.
5
FOXC1 and FOXC2 regulate growth plate chondrocyte maturation towards hypertrophy in the embryonic mouse limb skeleton.FOXC1 和 FOXC2 调节胚胎鼠肢骨骼生长板软骨细胞向肥大成熟的方向分化。
Development. 2024 Aug 15;151(16). doi: 10.1242/dev.202798. Epub 2024 Aug 22.
6
A comprehensive review and advanced biomolecule-based therapies for osteoporosis.骨质疏松症的综合综述及基于生物分子的先进疗法。
J Adv Res. 2025 May;71:337-354. doi: 10.1016/j.jare.2024.05.024. Epub 2024 May 27.
7
Hyperthyroidism-driven bone loss depends on BMP receptor Bmpr1a expression in osteoblasts.甲状腺功能亢进症引起的骨质流失依赖于成骨细胞中 BMP 受体 Bmpr1a 的表达。
Commun Biol. 2024 May 8;7(1):548. doi: 10.1038/s42003-024-06227-0.
8
Bone Substitute Options for Spine Fusion in Patients With Spine Trauma-Part II: The Role of rhBMP.脊柱创伤患者脊柱融合的骨替代选择 - 第二部分:重组人骨形态发生蛋白的作用
Korean J Neurotrauma. 2024 Mar 21;20(1):35-44. doi: 10.13004/kjnt.2024.20.e13. eCollection 2024 Mar.
9
Advances with Platelet-Rich Plasma for Bone Healing.富含血小板血浆促进骨愈合的研究进展
Biologics. 2024 Jan 25;18:29-59. doi: 10.2147/BTT.S290341. eCollection 2024.
10
Unique macrophage phenotypes activated by BMP signaling in breast cancer bone metastases.乳腺癌骨转移中 BMP 信号激活的独特巨噬细胞表型。
JCI Insight. 2024 Jan 9;9(1):e168517. doi: 10.1172/jci.insight.168517.
红骨髓祖细胞产生破骨细胞群体,有助于骨内稳态和修复。
Nat Cell Biol. 2020 Jan;22(1):49-59. doi: 10.1038/s41556-019-0437-8. Epub 2020 Jan 6.
4
Activin A receptor type 1-mediated BMP signaling regulates RANKL-induced osteoclastogenesis via canonical SMAD-signaling pathway.激活素 A 受体型 1 介导的 BMP 信号通过经典 SMAD 信号通路调节 RANKL 诱导的破骨细胞生成。
J Biol Chem. 2019 Nov 22;294(47):17818-17836. doi: 10.1074/jbc.RA119.009521. Epub 2019 Oct 16.
5
Developmental origin, functional maintenance and genetic rescue of osteoclasts.破骨细胞的发育起源、功能维持和遗传修复。
Nature. 2019 Apr;568(7753):541-545. doi: 10.1038/s41586-019-1105-7. Epub 2019 Apr 10.
6
Bone morphogenetic proteins in fracture repair.骨折修复中的骨形态发生蛋白
Int Orthop. 2018 Nov;42(11):2619-2626. doi: 10.1007/s00264-018-4153-y. Epub 2018 Sep 15.
7
SMAD1/5 signaling in osteoclasts regulates bone formation via coupling factors.破骨细胞中的 SMAD1/5 信号通过耦联因子调节骨形成。
PLoS One. 2018 Sep 6;13(9):e0203404. doi: 10.1371/journal.pone.0203404. eCollection 2018.
8
The BMP Pathway and Its Inhibitors in the Skeleton.BMP 通路及其在骨骼中的抑制剂。
Physiol Rev. 2018 Oct 1;98(4):2431-2452. doi: 10.1152/physrev.00028.2017.
9
Pharmacologic Calcitriol Inhibits Osteoclast Lineage Commitment via the BMP-Smad1 and IκB-NF-κB Pathways.药理活性骨化三醇通过骨形态发生蛋白-Smad1和IκB-核因子κB信号通路抑制破骨细胞谱系定向分化。
J Bone Miner Res. 2017 Jul;32(7):1406-1420. doi: 10.1002/jbmr.3146. Epub 2017 May 9.
10
Smad4 is required to inhibit osteoclastogenesis and maintain bone mass.Smad4是抑制破骨细胞生成和维持骨量所必需的。
Sci Rep. 2016 Oct 12;6:35221. doi: 10.1038/srep35221.