• 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

髁突软骨过度负荷应激诱导的进行性退变和自我修复。

Overloading stress-induced progressive degeneration and self-repair in condylar cartilage.

机构信息

Department of Orthodontics, Stomatological Hospital of Chongqing Medical University, Chongqing, China.

Chongqing Key Laboratory of Oral Disease and Biomedical Sciences, Stomatological Hospital of Chongqing Medical University, Chongqing, China.

出版信息

Ann N Y Acad Sci. 2021 Nov;1503(1):72-87. doi: 10.1111/nyas.14606. Epub 2021 May 7.

DOI:10.1111/nyas.14606
PMID:33962484
Abstract

Overloading stress-induced condylar cartilage degeneration acts as the main pathologic change in temporomandibular joint osteoarthritis (TMJ-OA). However, the progression of degeneration and the ability for self-repair remain poorly understood. Here, we explored the progression of cartilage degeneration by dividing pathological stages using a steady mouth-opening mouse model. Then, we observed changes of cartilage by removing the loading at different stages to test the potential self-repair after degeneration induced. Three-dimensional confocal microscopy combined with histology and micro-CT scanning was applied to examine TMJ at different stages of degeneration before and after self-repair. We found the cartilage underwent progressive and thorough degeneration as the overloading stress developed. During the initial adaptation stage, robust proliferation of posteromedial cartilage began at the area of direct loading. Subsequently, widespread chondrocyte apoptosis was found, followed by new chondrocyte proliferation in aggregates with matrix degradation and subchondral bone catabolism. Finally, with cartilage surface damage, the degeneration reached a point where the lesion could not be reversed by self-repair. While the cartilage nearly returned to normal when the interference was removed within 5 days. These results suggested overloading force induces a pathological process of successive degeneration in TMJ cartilage, which can be reversed by self-repair at early stages.

摘要

加载压力诱导的髁突软骨退变是颞下颌关节骨关节炎(TMJ-OA)的主要病理变化。然而,退变的进展和自我修复能力仍知之甚少。在这里,我们通过使用稳定张口的小鼠模型将病理阶段进行划分,从而探索软骨退变的进展。然后,我们在不同阶段去除负荷以观察退变后软骨的潜在自我修复能力。三维共聚焦显微镜结合组织学和微 CT 扫描用于检查退变前后不同阶段的 TMJ。我们发现随着加载压力的增加,软骨经历了进行性和彻底的退变。在初始适应阶段,直接加载区域的髁突后内侧软骨开始大量增殖。随后,广泛的软骨细胞凋亡,随后在基质降解和软骨下骨代谢的聚集中有新的软骨细胞增殖。最后,由于软骨表面损伤,退变达到了自我修复无法逆转的程度。然而,当在 5 天内去除干扰时,软骨几乎恢复正常。这些结果表明,加载力在 TMJ 软骨中诱导了一个连续退变的病理过程,在早期阶段可以通过自我修复来逆转。

相似文献

1
Overloading stress-induced progressive degeneration and self-repair in condylar cartilage.髁突软骨过度负荷应激诱导的进行性退变和自我修复。
Ann N Y Acad Sci. 2021 Nov;1503(1):72-87. doi: 10.1111/nyas.14606. Epub 2021 May 7.
2
Pathological mechanism of chondrocytes and the surrounding environment during osteoarthritis of temporomandibular joint.颞下颌关节骨关节炎中软骨细胞及周围环境的病理机制。
J Cell Mol Med. 2021 Jun;25(11):4902-4911. doi: 10.1111/jcmm.16514. Epub 2021 May 5.
3
Development of a Rat Model of Mechanically Induced Tunable Pain and Associated Temporomandibular Joint Responses.机械诱导可调性疼痛大鼠模型及相关颞下颌关节反应的建立
J Oral Maxillofac Surg. 2016 Jan;74(1):54.e1-10. doi: 10.1016/j.joms.2015.09.005. Epub 2015 Sep 21.
4
Differential effects of high-physiological oestrogen on the degeneration of mandibular condylar cartilage and subchondral bone.高生理雌激素对下颌髁突软骨和软骨下骨退变的影响差异。
Bone. 2018 Jun;111:9-22. doi: 10.1016/j.bone.2018.03.008. Epub 2018 Mar 10.
5
A repetitive, steady mouth opening induced an osteoarthritis-like lesion in the rabbit temporomandibular joint.重复性的、稳定的张口动作在兔颞下颌关节中诱发了类似骨关节炎的病变。
J Dent Res. 2003 Sep;82(9):731-5. doi: 10.1177/154405910308200914.
6
Roles of hypoxia inducible factor-1α in the temporomandibular joint.缺氧诱导因子-1α在颞下颌关节中的作用。
Arch Oral Biol. 2017 Jan;73:274-281. doi: 10.1016/j.archoralbio.2016.10.028. Epub 2016 Oct 28.
7
Progression of cartilage degradation, bone resorption and pain in rat temporomandibular joint osteoarthritis induced by injection of iodoacetate.碘乙酸注射诱导大鼠颞下颌关节骨关节炎中软骨降解、骨吸收和疼痛的进展。
PLoS One. 2012;7(9):e45036. doi: 10.1371/journal.pone.0045036. Epub 2012 Sep 11.
8
Rebamipide Attenuates Mandibular Condylar Degeneration in a Murine Model of TMJ-OA by Mediating a Chondroprotective Effect and by Downregulating RANKL-Mediated Osteoclastogenesis.瑞巴派特通过介导软骨保护作用和下调RANKL介导的破骨细胞生成,减轻颞下颌关节骨关节炎小鼠模型中的下颌髁突退变。
PLoS One. 2016 Apr 28;11(4):e0154107. doi: 10.1371/journal.pone.0154107. eCollection 2016.
9
MTORC1 coordinates the autophagy and apoptosis signaling in articular chondrocytes in osteoarthritic temporomandibular joint.骨关节炎颞下颌关节中软骨细胞的 MTORC1 协调自噬和细胞凋亡信号。
Autophagy. 2020 Feb;16(2):271-288. doi: 10.1080/15548627.2019.1606647. Epub 2019 Apr 21.
10
Receptor-interacting protein 1 inhibition prevents mechanical stress-induced temporomandibular joint osteoarthritis by regulating apoptosis and later-stage necroptosis of chondrocytes.受体相互作用蛋白 1 抑制通过调节软骨细胞凋亡和晚期坏死性凋亡来预防机械应激诱导的颞下颌关节骨关节炎。
Arch Oral Biol. 2023 Mar;147:105612. doi: 10.1016/j.archoralbio.2022.105612. Epub 2022 Dec 28.

引用本文的文献

1
Mechanistic Insights Into Overloading-Induced Terminal Differentiation of TMJ Condylar Cartilage at the Single Cell Level.在单细胞水平上对颞下颌关节髁突软骨过载诱导终末分化的机制性见解
Smart Med. 2025 Jul 30;4(3):e70011. doi: 10.1002/smmd.70011. eCollection 2025 Sep.
2
Human Dental Follicle Cell-Derived Small Extracellular Vesicles Attenuate Temporomandibular Joint Cartilage Damage through Inhibiting HIF-2.人牙囊细胞衍生的小细胞外囊泡通过抑制缺氧诱导因子-2减轻颞下颌关节软骨损伤
J Tissue Eng Regen Med. 2023 Sep 25;2023:6625123. doi: 10.1155/2023/6625123. eCollection 2023.
3
Bioprinting techniques for regeneration of oral and craniofacial tissues: Current advances and future prospects.
用于口腔和颅面组织再生的生物打印技术:当前进展与未来前景
J Oral Biol Craniofac Res. 2025 Mar-Apr;15(2):331-346. doi: 10.1016/j.jobcr.2025.01.019. Epub 2025 Feb 12.
4
Phosphotungstic acid-enhanced micro-computed tomography and RNA sequencing provide a new perspective on temporomandibular joint arthritis induced by complete Freund's adjuvant and collagen-induced arthritis in rat models.磷钨酸增强型微计算机断层扫描和RNA测序为完全弗氏佐剂和胶原诱导的大鼠颞下颌关节关节炎模型提供了新的视角。
J Dent Sci. 2025 Jan;20(1):189-200. doi: 10.1016/j.jds.2024.08.014. Epub 2024 Aug 28.
5
Sulfur-species in Zinc-specific Condylar Zones of a Rat Temporomandibular Joint.大鼠颞下颌关节锌特异性髁突区中的硫物种
bioRxiv. 2024 Nov 14:2024.11.11.623079. doi: 10.1101/2024.11.11.623079.
6
Unveiling MRI-based structural phenotypes in temporomandibular joint osteoarthritis: implications for clinical practice and research.揭示磁共振成像(MRI)在颞下颌关节骨关节炎中的结构表型:对临床实践和研究的启示。
Dental Press J Orthod. 2024 Sep 2;29(4):e24spe4. doi: 10.1590/2177-6709.29.4.e24spe4. eCollection 2024.
7
Excessive load promotes temporomandibular joint chondrocyte apoptosis via Piezo1/endoplasmic reticulum stress pathway.过度负荷通过 Piezo1/内质网应激途径促进颞下颌关节软骨细胞凋亡。
J Cell Mol Med. 2024 Jun;28(11):e18472. doi: 10.1111/jcmm.18472.
8
Unilateral high-riding vertebral artery is associated with asymmetric morphological changes of the atlantoaxial joint: a novel risk factor for atlantoaxial osteoarthritis.单侧椎动脉高位走行与寰枢关节形态不对称改变相关:寰枢椎骨关节炎的一个新危险因素。
Eur Spine J. 2024 Jun;33(6):2322-2331. doi: 10.1007/s00586-024-08285-8. Epub 2024 Apr 27.
9
Conditioned Medium From Stem Cells of Human Exfoliated Deciduous Teeth Alleviates Mouse Osteoarthritis by Inducing sFRP1-Expressing M2 Macrophages.人乳牙干细胞条件培养基通过诱导表达sFRP1的M2巨噬细胞减轻小鼠骨关节炎
Stem Cells Transl Med. 2024 Apr 15;13(4):399-413. doi: 10.1093/stcltm/szae006.
10
Fabrication of novel nanofiber composed of gelatin/alginate with zirconium oxide NPs regulate orthodontic progression of cartilage degeneration on Wnt/β-catenin signaling axis in MC3T3-E1 cells.由明胶/藻酸盐与氧化锆纳米颗粒组成的新型纳米纤维的制备可调节MC3T3-E1细胞中Wnt/β-连环蛋白信号轴上软骨退变的正畸进展。
Regen Ther. 2024 Feb 2;25:308-319. doi: 10.1016/j.reth.2024.01.004. eCollection 2024 Mar.