Divergent trajectories of structural accrual and matrix-level mechanical properties during alveolar bone maturation.

IF 3.5 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Jun Zhou, Xiaoling Liao, Jingxiao Zhong, Li Zhou, Chie Watanabe, Reina Tanaka, Lu Sun, Yasutaka Sugamori, Jiaming Zhang, Yo Shibata, Zailing Gong
{"title":"Divergent trajectories of structural accrual and matrix-level mechanical properties during alveolar bone maturation.","authors":"Jun Zhou, Xiaoling Liao, Jingxiao Zhong, Li Zhou, Chie Watanabe, Reina Tanaka, Lu Sun, Yasutaka Sugamori, Jiaming Zhang, Yo Shibata, Zailing Gong","doi":"10.1007/s00223-026-01615-6","DOIUrl":null,"url":null,"abstract":"<p><p>Alveolar bone, a highly dynamic tissue supporting dentition, undergoes a poorly characterized transition from growth to maturity that is critical for orthodontic treatment and periodontal risk assessment. We integrated micro‑CT (μCT), nanoindentation creep modeling, and RNA sequencing to define structural, mechanical, and transcriptomic signatures of this transition in rats at 12 and 24 weeks, using the molar‑bearing alveolar region (M1) and the mandibular notch as a non‑alveolar reference. μCT revealed progressive cortical and trabecular bone accrual at 24 weeks, with trabeculae shifting from rod‑like to plate‑like configurations via lateral expansion. Nanoindentation revealed a site-specific decreasing trend in elastic modulus at M1, which was absent at the mandibular notch, suggesting a regional divergence of local mechanics from bulk mineralization. Time‑dependent creep analysis demonstrated that fast retardation time τ₁ tended to increase at the notch but remained stable at M1, while long‑timescale τ₂ showed a similar upward tendency at the notch, suggesting a viscosity‑related shift in viscoelastic behavior confined to the notch. Transcriptomically, 24‑week alveolar bone exhibited downregulation of genes related to bone matrix assembly and mineralization, alongside observed enrichment of senescence and inflammatory pathways. These molecular changes offer biological context for the observed divergence between continued structural bone accrual and altered matrix-level mechanical quality. Collectively, our findings demonstrate that alveolar bone maturation involves distinct trajectories of structural accrual and site-specific matrix alterations, providing important considerations for the biomechanical assessment of dynamic skeletal tissues.</p>","PeriodicalId":9601,"journal":{"name":"Calcified Tissue International","volume":"117 1","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Calcified Tissue International","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00223-026-01615-6","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0

Abstract

Alveolar bone, a highly dynamic tissue supporting dentition, undergoes a poorly characterized transition from growth to maturity that is critical for orthodontic treatment and periodontal risk assessment. We integrated micro‑CT (μCT), nanoindentation creep modeling, and RNA sequencing to define structural, mechanical, and transcriptomic signatures of this transition in rats at 12 and 24 weeks, using the molar‑bearing alveolar region (M1) and the mandibular notch as a non‑alveolar reference. μCT revealed progressive cortical and trabecular bone accrual at 24 weeks, with trabeculae shifting from rod‑like to plate‑like configurations via lateral expansion. Nanoindentation revealed a site-specific decreasing trend in elastic modulus at M1, which was absent at the mandibular notch, suggesting a regional divergence of local mechanics from bulk mineralization. Time‑dependent creep analysis demonstrated that fast retardation time τ₁ tended to increase at the notch but remained stable at M1, while long‑timescale τ₂ showed a similar upward tendency at the notch, suggesting a viscosity‑related shift in viscoelastic behavior confined to the notch. Transcriptomically, 24‑week alveolar bone exhibited downregulation of genes related to bone matrix assembly and mineralization, alongside observed enrichment of senescence and inflammatory pathways. These molecular changes offer biological context for the observed divergence between continued structural bone accrual and altered matrix-level mechanical quality. Collectively, our findings demonstrate that alveolar bone maturation involves distinct trajectories of structural accrual and site-specific matrix alterations, providing important considerations for the biomechanical assessment of dynamic skeletal tissues.

牙槽骨成熟过程中结构累积和基质水平力学特性的不同轨迹。
牙槽骨是一种高度动态的支持牙列的组织,从生长到成熟的转变特征不明显,这对正畸治疗和牙周风险评估至关重要。我们整合了微CT (μCT)、纳米压痕蠕变模型和RNA测序来定义大鼠在12周和24周时这种转变的结构、机械和转录组特征,使用磨牙牙槽区(M1)和下颌切迹作为非牙槽区参考。μCT显示24周时皮质骨和骨小梁增生,骨小梁通过外侧扩张从棒状变为板状。纳米压痕在M1处的弹性模量有降低的趋势,而在下颌切迹处没有,表明局部力学与整体矿化存在区域性差异。时间相关的蠕变分析表明,快速延迟时间τ 1在缺口处趋于增加,但在M1处保持稳定,而长时间尺度τ 2在缺口处表现出类似的上升趋势,表明粘弹性行为仅限于缺口的粘度相关转移。转录组学上,24周的牙槽骨表现出与骨基质组装和矿化相关的基因下调,同时观察到衰老和炎症途径的富集。这些分子变化为观察到的持续的骨结构累积和改变的基质水平机械质量之间的差异提供了生物学背景。总的来说,我们的研究结果表明,牙槽骨成熟涉及结构累积和特定部位基质改变的不同轨迹,为动态骨组织的生物力学评估提供了重要的考虑因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Calcified Tissue International
Calcified Tissue International 医学-内分泌学与代谢
CiteScore
8.00
自引率
2.40%
发文量
112
审稿时长
4-8 weeks
期刊介绍: Calcified Tissue International and Musculoskeletal Research publishes original research and reviews concerning the structure and function of bone, and other musculoskeletal tissues in living organisms and clinical studies of musculoskeletal disease. It includes studies of cell biology, molecular biology, intracellular signalling, and physiology, as well as research into the hormones, cytokines and other mediators that influence the musculoskeletal system. The journal also publishes clinical studies of relevance to bone disease, mineral metabolism, muscle function, and musculoskeletal interactions.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书