• 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

骨折愈合的细胞生物学。

Cellular biology of fracture healing.

机构信息

Department of Orthopaedic Surgery, University of California at San Francisco, San Francisco, California.

Department of Physiology, College of Osteopathic Medicine, Michigan State University, East Lansing, Michigan.

出版信息

J Orthop Res. 2019 Jan;37(1):35-50. doi: 10.1002/jor.24170. Epub 2018 Nov 30.

DOI:10.1002/jor.24170
PMID:30370699
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6542569/
Abstract

The biology of bone healing is a rapidly developing science. Advances in transgenic and gene-targeted mice have enabled tissue and cell-specific investigations of skeletal regeneration. As an example, only recently has it been recognized that chondrocytes convert to osteoblasts during healing bone, and only several years prior, seminal publications reported definitively that the primary tissues contributing bone forming cells during regeneration were the periosteum and endosteum. While genetically modified animals offer incredible insights into the temporal and spatial importance of various gene products, the complexity and rapidity of healing-coupled with the heterogeneity of animal models-renders studies of regenerative biology challenging. Herein, cells that play a key role in bone healing will be reviewed and extracellular mediators regulating their behavior discussed. We will focus on recent studies that explore novel roles of inflammation in bone healing, and the origins and fates of various cells in the fracture environment. © 2018 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res.

摘要

骨愈合生物学是一门快速发展的科学。转基因和基因靶向小鼠的进步使骨骼再生的组织和细胞特异性研究成为可能。例如,直到最近才认识到软骨细胞在骨愈合过程中转化为成骨细胞,而就在几年前,开创性的出版物明确报道,在再生过程中形成骨细胞的主要组织是骨膜和骨内膜。虽然转基因动物为研究各种基因产物的时间和空间重要性提供了令人难以置信的见解,但愈合的复杂性和快速性以及动物模型的异质性使得再生生物学的研究具有挑战性。本文将对在骨愈合中起关键作用的细胞进行综述,并讨论调节其行为的细胞外介质。我们将重点介绍最近的研究,这些研究探索了炎症在骨愈合中的新作用,以及骨折环境中各种细胞的起源和命运。版权所有©2018 矫形研究协会。由 Wiley Periodicals,Inc. 出版。J 矫形研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d925/6542569/2d4f6db1c017/nihms-1024877-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d925/6542569/cfb39a7806a4/nihms-1024877-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d925/6542569/d309116b5fc0/nihms-1024877-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d925/6542569/9844542b6b1b/nihms-1024877-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d925/6542569/a6e1d07b99df/nihms-1024877-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d925/6542569/2d4f6db1c017/nihms-1024877-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d925/6542569/cfb39a7806a4/nihms-1024877-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d925/6542569/d309116b5fc0/nihms-1024877-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d925/6542569/9844542b6b1b/nihms-1024877-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d925/6542569/a6e1d07b99df/nihms-1024877-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d925/6542569/2d4f6db1c017/nihms-1024877-f0005.jpg

相似文献

1
Cellular biology of fracture healing.骨折愈合的细胞生物学。
J Orthop Res. 2019 Jan;37(1):35-50. doi: 10.1002/jor.24170. Epub 2018 Nov 30.
2
Cartilage to bone transformation during fracture healing is coordinated by the invading vasculature and induction of the core pluripotency genes.骨折愈合过程中软骨向骨的转变由侵入的脉管系统和核心多能性基因的诱导协调。
Development. 2017 Jan 15;144(2):221-234. doi: 10.1242/dev.130807.
3
Osteoclast depletion with clodronate liposomes delays fracture healing in mice.用氯膦酸盐脂质体清除破骨细胞会延迟小鼠骨折愈合。
J Orthop Res. 2017 Aug;35(8):1699-1706. doi: 10.1002/jor.23440. Epub 2016 Oct 6.
4
Suppression of Notch Signaling in Osteoclasts Improves Bone Regeneration and Healing.破骨细胞中 Notch 信号的抑制可改善骨再生和愈合。
J Orthop Res. 2019 Oct;37(10):2089-2103. doi: 10.1002/jor.24384. Epub 2019 Jun 24.
5
Effects of Aging on Fracture Healing.衰老对骨折愈合的影响。
Curr Osteoporos Rep. 2017 Dec;15(6):601-608. doi: 10.1007/s11914-017-0413-9.
6
Endostatin inhibits Callus remodeling during fracture healing in mice.内皮抑素抑制小鼠骨折愈合过程中的骨痂重塑。
J Orthop Res. 2013 Oct;31(10):1579-84. doi: 10.1002/jor.22401. Epub 2013 May 30.
7
Role of bone regeneration and turnover modulators in control of fracture.骨再生和转换调节剂在骨折控制中的作用。
Crit Rev Eukaryot Gene Expr. 2007;17(3):197-213. doi: 10.1615/critreveukargeneexpr.v17.i3.30.
8
Osteogenic Differentiation of Periosteal Cells During Fracture Healing.骨折愈合过程中骨膜细胞的成骨分化
J Cell Physiol. 2017 May;232(5):913-921. doi: 10.1002/jcp.25641. Epub 2016 Oct 26.
9
Skeletal stem and progenitor cells in bone development and repair.骨骼中的干细胞和祖细胞在骨骼发育和修复中的作用。
J Bone Miner Res. 2024 Jul 23;39(6):633-654. doi: 10.1093/jbmr/zjae069.
10
The cell and molecular biology of fracture healing.骨折愈合的细胞与分子生物学
Clin Orthop Relat Res. 1998 Oct(355 Suppl):S7-21. doi: 10.1097/00003086-199810001-00003.

引用本文的文献

1
Deep behavioral phenotyping tracks functional recovery following tibia fracture in mice.深度行为表型分析追踪小鼠胫骨骨折后的功能恢复情况。
Front Physiol. 2025 Aug 26;16:1630155. doi: 10.3389/fphys.2025.1630155. eCollection 2025.
2
The Role of Sirtuins in Bone Repair From the Perspective of Glucose Metabolism.从葡萄糖代谢角度看沉默调节蛋白在骨修复中的作用
Int J Gen Med. 2025 Sep 1;18:5013-5031. doi: 10.2147/IJGM.S530523. eCollection 2025.
3
Serum bone turnover biomarkers in early postoperative period related to the spontaneous resolution of disc herniation.

本文引用的文献

1
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.
2
Complement receptors C5aR1 and C5aR2 act differentially during the early immune response after bone fracture but are similarly involved in bone repair.补体受体 C5aR1 和 C5aR2 在骨折后早期免疫反应中发挥不同作用,但在骨修复中具有相似的作用。
Sci Rep. 2017 Oct 25;7(1):14061. doi: 10.1038/s41598-017-14444-3.
3
Bone healing in an aged murine fracture model is characterized by sustained callus inflammation and decreased cell proliferation.
术后早期血清骨转换生物标志物与椎间盘突出症的自然缓解相关。
Sci Rep. 2025 Sep 2;15(1):32279. doi: 10.1038/s41598-025-17518-9.
4
Efficacy of biomarkers in the endochondral phase of fracture repair and healing in long bones: A clinical observational studys.生物标志物在长骨骨折修复与愈合软骨内成骨阶段的疗效:一项临床观察研究
PLoS Med. 2025 Aug 29;22(8):e1004640. doi: 10.1371/journal.pmed.1004640. eCollection 2025 Aug.
5
Overactivation of EGFR signaling in skeletal stem/progenitor cells promotes bone formation and repair.骨骼干/祖细胞中表皮生长因子受体(EGFR)信号的过度激活可促进骨形成和修复。
Theranostics. 2025 Jul 24;15(16):8117-8136. doi: 10.7150/thno.115406. eCollection 2025.
6
Early cellular events of osteomucosal healing in the tooth extraction socket.拔牙窝骨黏膜愈合的早期细胞事件。
PLoS One. 2025 Aug 14;20(8):e0328459. doi: 10.1371/journal.pone.0328459. eCollection 2025.
7
3D printed scaffolds loaded with BMP-2 for bone defect regeneration: a systematic review and meta-analysis.用于骨缺损再生的负载骨形态发生蛋白-2的3D打印支架:系统评价与荟萃分析
Front Physiol. 2025 Jul 30;16:1641937. doi: 10.3389/fphys.2025.1641937. eCollection 2025.
8
Single-cell profiling reveals periosteal signatures of impaired periosteal cells proliferation in a drill-hole model of type 2 diabetes.单细胞分析揭示了2型糖尿病钻孔模型中骨膜细胞增殖受损的骨膜特征。
Cell Commun Signal. 2025 Aug 12;23(1):371. doi: 10.1186/s12964-025-02349-y.
9
Associations between an inflammatory diet index and nonunion: a prospective study of 172,839 UK biobank participants.炎症饮食指数与骨不连之间的关联:对172,839名英国生物银行参与者的前瞻性研究。
Front Nutr. 2025 Jul 14;12:1640259. doi: 10.3389/fnut.2025.1640259. eCollection 2025.
10
The effects of Cissus quadrangularis on bone-related biomarkers in humans: a systematic review and meta-analysis.四角金虎尾对人体骨相关生物标志物的影响:一项系统评价和荟萃分析。
BMC Complement Med Ther. 2025 Jul 24;25(1):286. doi: 10.1186/s12906-025-04995-8.
老年小鼠骨折模型中的骨愈合以持续的骨痂炎症和细胞增殖减少为特征。
J Orthop Res. 2018 Jan;36(1):149-158. doi: 10.1002/jor.23652. Epub 2017 Oct 9.
4
Pro-inflammatory M1 macrophages promote Osteogenesis by mesenchymal stem cells via the COX-2-prostaglandin E2 pathway.促炎性M1巨噬细胞通过COX-2-前列腺素E2途径促进间充质干细胞的成骨作用。
J Orthop Res. 2017 Nov;35(11):2378-2385. doi: 10.1002/jor.23553. Epub 2017 Mar 13.
5
TRPV1 deletion impaired fracture healing and inhibited osteoclast and osteoblast differentiation.TRPV1 缺失会损害骨折愈合,并抑制破骨细胞和成骨细胞分化。
Sci Rep. 2017 Feb 22;7:42385. doi: 10.1038/srep42385.
6
Cartilage to bone transformation during fracture healing is coordinated by the invading vasculature and induction of the core pluripotency genes.骨折愈合过程中软骨向骨的转变由侵入的脉管系统和核心多能性基因的诱导协调。
Development. 2017 Jan 15;144(2):221-234. doi: 10.1242/dev.130807.
7
IL-17-producing γδ T cells enhance bone regeneration.产生白细胞介素-17的γδ T细胞可促进骨再生。
Nat Commun. 2016 Mar 11;7:10928. doi: 10.1038/ncomms10928.
8
NOTCH signaling in skeletal progenitors is critical for fracture repair.骨骼祖细胞中的NOTCH信号传导对骨折修复至关重要。
J Clin Invest. 2016 Apr 1;126(4):1471-81. doi: 10.1172/JCI80672. Epub 2016 Mar 7.
9
Fracture Healing Is Delayed in Immunodeficient NOD/scid‑IL2Rγcnull Mice.免疫缺陷的NOD/scid-IL2Rγc基因敲除小鼠的骨折愈合延迟。
PLoS One. 2016 Feb 5;11(2):e0147465. doi: 10.1371/journal.pone.0147465. eCollection 2016.
10
Fibrinolysis is essential for fracture repair and prevention of heterotopic ossification.纤维蛋白溶解对于骨折修复和预防异位骨化至关重要。
J Clin Invest. 2015 Sep;125(9):3723. doi: 10.1172/JCI84059. Epub 2015 Sep 1.