• 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

衰老对骨骼的影响。

Consequences of Aging on Bone.

机构信息

College of Athletic Performance, Shanghai University of Sport, Shanghai, China.

School of Exercise and Health, Shanghai University of Sport, Shanghai, China.

出版信息

Aging Dis. 2023 Nov 20;15(6):2417-2452. doi: 10.14336/AD.2023.1115.

DOI:10.14336/AD.2023.1115
PMID:38029404
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11567267/
Abstract

With the aging of the global population, the incidence of musculoskeletal diseases has been increasing, seriously affecting people's health. As people age, the microenvironment within skeleton favors bone resorption and inhibits bone formation, accompanied by bone marrow fat accumulation and multiple cellular senescence. Specifically, skeletal stem/stromal cells (SSCs) during aging tend to undergo adipogenesis rather than osteogenesis. Meanwhile, osteoblasts, as well as osteocytes, showed increased apoptosis, decreased quantity, and multiple functional limitations including impaired mechanical sensing, intercellular modulation, and exosome secretion. Also, the bone resorption function of macrophage-lineage cells (including osteoclasts and preosteoclasts) was significantly enhanced, as well as impaired vascularization and innervation. In this study, we systematically reviewed the effect of aging on bone and the within microenvironment (including skeletal cells as well as their intracellular structure variations, vascular structures, innervation, marrow fat distribution, and lymphatic system) caused by aging, and mechanisms of osteoimmune regulation of the bone environment in the aging state, and the causal relationship with multiple musculoskeletal diseases in addition with their potential therapeutic strategy.

摘要

随着全球人口老龄化,肌肉骨骼疾病的发病率不断上升,严重影响人们的健康。随着年龄的增长,骨骼内的微环境有利于骨质吸收而抑制骨质形成,同时伴有骨髓脂肪积累和多种细胞衰老。具体来说,衰老过程中的骨骼干/基质细胞(SSCs)倾向于发生脂肪生成而不是成骨。同时,成骨细胞和破骨细胞的凋亡增加,数量减少,并且存在多种功能限制,包括机械感知、细胞间调节和外泌体分泌受损。此外,巨噬细胞谱系细胞(包括破骨细胞和前破骨细胞)的骨质吸收功能显著增强,同时血管生成和神经支配受损。在这项研究中,我们系统地回顾了衰老对骨骼和衰老引起的微环境(包括骨骼细胞及其细胞内结构变化、血管结构、神经支配、骨髓脂肪分布和淋巴系统)的影响,以及衰老状态下骨环境的骨免疫调节机制,以及与多种肌肉骨骼疾病的因果关系及其潜在的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcb/11567267/cd3447e36b2e/AD-15-6-2417-g8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcb/11567267/64c9135f323c/AD-15-6-2417-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcb/11567267/4b46487331c4/AD-15-6-2417-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcb/11567267/85f5162545bb/AD-15-6-2417-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcb/11567267/730d395e74a0/AD-15-6-2417-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcb/11567267/89c2c6d19870/AD-15-6-2417-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcb/11567267/a62cb68e018f/AD-15-6-2417-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcb/11567267/77d7184f8f8f/AD-15-6-2417-g7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcb/11567267/cd3447e36b2e/AD-15-6-2417-g8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcb/11567267/64c9135f323c/AD-15-6-2417-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcb/11567267/4b46487331c4/AD-15-6-2417-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcb/11567267/85f5162545bb/AD-15-6-2417-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcb/11567267/730d395e74a0/AD-15-6-2417-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcb/11567267/89c2c6d19870/AD-15-6-2417-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcb/11567267/a62cb68e018f/AD-15-6-2417-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcb/11567267/77d7184f8f8f/AD-15-6-2417-g7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dcb/11567267/cd3447e36b2e/AD-15-6-2417-g8.jpg

相似文献

1
Consequences of Aging on Bone.衰老对骨骼的影响。
Aging Dis. 2023 Nov 20;15(6):2417-2452. doi: 10.14336/AD.2023.1115.
2
Prescription of Controlled Substances: Benefits and Risks管制药品的处方:益处与风险
3
Enhanced fatty acid oxidation in osteoprogenitor cells provides protection from high-fat diet induced bone dysfunction.骨祖细胞中脂肪酸氧化增强可预防高脂饮食诱导的骨功能障碍。
J Bone Miner Res. 2025 Feb 2;40(2):283-298. doi: 10.1093/jbmr/zjae195.
4
Are osteoblasts multiple cell types? A new diversity in skeletal stem cells and their derivatives.成骨细胞是多种细胞类型吗?骨骼干细胞及其衍生物的新多样性。
J Bone Miner Res. 2024 Sep 26;39(10):1386-1392. doi: 10.1093/jbmr/zjae109.
5
Depletion of marrow adipo-CAR cells in mice enhances bone formation by activating bone morphogenetic protein receptor (BMPR) in pre-osteoblasts.小鼠骨髓脂肪CAR细胞的消耗通过激活前成骨细胞中的骨形态发生蛋白受体(BMPR)来增强骨形成。
J Bone Miner Res. 2025 May 24;40(5):688-698. doi: 10.1093/jbmr/zjaf051.
6
DNA hydroxy methylases Tet1 and Tet2 regulate bone aging and bone marrow stromal cell metabolism through the IGF-1/mTOR signaling axis.DNA羟甲基化酶Tet1和Tet2通过IGF-1/mTOR信号轴调节骨骼衰老和骨髓基质细胞代谢。
Stem Cells. 2025 Jul 21;43(8). doi: 10.1093/stmcls/sxaf026.
7
Divergent effects of premineralization and prevascularization on osteogenesis and vascular integration in humanized tissue engineered bone constructs.矿化前和血管化前对人源化组织工程骨构建体中骨生成和血管整合的不同影响。
Acta Biomater. 2025 Jun 11. doi: 10.1016/j.actbio.2025.06.019.
8
Calorie restriction in mice impairs cortical but not trabecular peak bone mass by suppressing bone remodeling.限制小鼠卡路里摄入通过抑制骨重建而损害皮质骨但不损害小梁骨的峰值骨量。
J Bone Miner Res. 2024 Aug 21;39(8):1188-1199. doi: 10.1093/jbmr/zjae104.
9
Systemic deficits in lipid homeostasis promote aging-associated impairments in B cell progenitor development.脂质稳态的全身性缺陷会促进B细胞祖细胞发育中与衰老相关的损伤。
Geroscience. 2025 Apr 15. doi: 10.1007/s11357-025-01594-w.
10
Exosomes derived from umbilical cord mesenchymal stem cells alleviate jaw bone marrow mesenchymal stem cells senescence and restore osteogenic differentiation potential.脐带间充质干细胞来源的外泌体可减轻颌骨骨髓间充质干细胞衰老并恢复成骨分化潜能。
Stem Cell Res Ther. 2025 Aug 29;16(1):475. doi: 10.1186/s13287-025-04587-w.

引用本文的文献

1
Epigenetic Regulation of Aging and its Rejuvenation.衰老及其逆转的表观遗传调控
MedComm (2020). 2025 Sep 1;6(9):e70369. doi: 10.1002/mco2.70369. eCollection 2025 Sep.
2
Exosomes derived from umbilical cord mesenchymal stem cells alleviate jaw bone marrow mesenchymal stem cells senescence and restore osteogenic differentiation potential.脐带间充质干细胞来源的外泌体可减轻颌骨骨髓间充质干细胞衰老并恢复成骨分化潜能。
Stem Cell Res Ther. 2025 Aug 29;16(1):475. doi: 10.1186/s13287-025-04587-w.
3
Advances in Nanotechnology Research in Food Production, Nutrition, and Health.

本文引用的文献

1
The Emerging Role of the Mitochondrial Respiratory Chain in Skeletal Aging.线粒体呼吸链在骨骼衰老中的新兴作用。
Aging Dis. 2024 Aug 1;15(4):1784-1812. doi: 10.14336/AD.2023.0924.
2
Altered Osteoblast Metabolism with Aging Results in Lipid Accumulation and Oxidative Stress Mediated Bone Loss.随着年龄的增长,成骨细胞代谢发生改变,导致脂质积累和氧化应激介导的骨丢失。
Aging Dis. 2024 Apr 1;15(2):767-786. doi: 10.14336/AD.2023.0510.
3
Single-Cell RNA-Sequencing Reveals the Skeletal Cellular Dynamics in Bone Repair and Osteoporosis.单细胞 RNA 测序揭示了骨修复和骨质疏松症中的骨骼细胞动态。
纳米技术在食品生产、营养与健康领域的研究进展。
Nutrients. 2025 Jul 26;17(15):2443. doi: 10.3390/nu17152443.
4
Addressing osteoblast senescence: Molecular pathways and the frontier of anti-ageing treatments.应对成骨细胞衰老:分子途径与抗衰老治疗前沿
Clin Transl Med. 2025 Jul;15(7):e70417. doi: 10.1002/ctm2.70417.
5
Health benefits of anthocyanins against age-related diseases.花青素对与年龄相关疾病的健康益处。
Front Nutr. 2025 Jun 20;12:1618072. doi: 10.3389/fnut.2025.1618072. eCollection 2025.
6
Association of Urinary Cadmium and Antimony with Osteoporosis Risk in Postmenopausal Brazilian Women: Insights from a 20 Metal(loid) Biomonitoring Study.巴西绝经后女性尿镉和锑与骨质疏松症风险的关联:来自一项20种金属(类金属)生物监测研究的见解
Toxics. 2025 Jun 10;13(6):489. doi: 10.3390/toxics13060489.
7
Protective Effect of Methyl Sulfonyl Methane on the Progression of Age-Induced Bone Loss by Regulating Oxidative Stress-Mediated Bone Resorption.甲基磺酰甲烷通过调节氧化应激介导的骨吸收对年龄诱导的骨质流失进展的保护作用。
Antioxidants (Basel). 2025 Feb 13;14(2):216. doi: 10.3390/antiox14020216.
8
Rejuvenation of Bone Marrow Mesenchymal Stem Cells: Mechanisms and Their Application in Senile Osteoporosis Treatment.骨髓间充质干细胞的年轻化:机制及其在老年性骨质疏松症治疗中的应用
Biomolecules. 2025 Feb 13;15(2):276. doi: 10.3390/biom15020276.
9
Are Dietary Patterns Relevant for Reducing the Risk of Fractures and Sarcopenia?饮食模式与降低骨折和肌肉减少症风险相关吗?
Curr Osteoporos Rep. 2025 Jan 23;23(1):7. doi: 10.1007/s11914-024-00899-7.
10
Oligomeric Proanthocyanidins Ameliorate Cadmium-Induced Senescence of Osteocytes Through Combating Oxidative Stress and Inflammation.低聚原花青素通过对抗氧化应激和炎症改善镉诱导的骨细胞衰老。
Antioxidants (Basel). 2024 Dec 12;13(12):1515. doi: 10.3390/antiox13121515.
Int J Mol Sci. 2023 Jun 6;24(12):9814. doi: 10.3390/ijms24129814.
4
Bone regeneration in inflammation with aging and cell-based immunomodulatory therapy.衰老炎症状态下的骨再生与基于细胞的免疫调节治疗
Inflamm Regen. 2023 May 25;43(1):29. doi: 10.1186/s41232-023-00279-1.
5
Pharmaceutical treatment of bone loss: From animal models and drug development to future treatment strategies.骨质流失的药物治疗:从动物模型与药物研发到未来治疗策略
Pharmacol Ther. 2023 Apr;244:108383. doi: 10.1016/j.pharmthera.2023.108383. Epub 2023 Mar 16.
6
Inflammation produced by senescent osteocytes mediates age-related bone loss.衰老的破骨细胞引发的炎症导致与年龄相关的骨量流失。
Front Immunol. 2023 Feb 6;14:1114006. doi: 10.3389/fimmu.2023.1114006. eCollection 2023.
7
Kidney tonifying traditional Chinese medicine: Potential implications for the prevention and treatment of osteoporosis.补肾中药:对骨质疏松症防治的潜在意义
Front Pharmacol. 2023 Jan 9;13:1063899. doi: 10.3389/fphar.2022.1063899. eCollection 2022.
8
Lymphatic vessels in bone support regeneration after injury.骨中的淋巴管支持损伤后的再生。
Cell. 2023 Jan 19;186(2):382-397.e24. doi: 10.1016/j.cell.2022.12.031.
9
Muscle-derived extracellular vesicles improve disuse-induced osteoporosis by rebalancing bone formation and bone resorption.肌肉来源的细胞外囊泡通过重新平衡骨形成和骨吸收来改善废用性骨质疏松症。
Acta Biomater. 2023 Feb;157:609-624. doi: 10.1016/j.actbio.2022.12.019. Epub 2022 Dec 13.
10
Network pharmacology-based strategy to investigate pharmacological mechanism of Liuwei Dihuang Pill against postmenopausal osteoporosis.基于网络药理学的策略探讨六味地黄丸治疗绝经后骨质疏松症的药理机制。
Medicine (Baltimore). 2022 Nov 25;101(47):e31387. doi: 10.1097/MD.0000000000031387.