M2 Macrophage-Derived Exosomes Promote Tendon-to-Bone Healing by Alleviating Cellular Senescence in Aged Rats.

Zhuochang Cai, Longqiang Shu, Chongyang Wang, Xuetao Xie, Xudong Liu
{"title":"M2 Macrophage-Derived Exosomes Promote Tendon-to-Bone Healing by Alleviating Cellular Senescence in Aged Rats.","authors":"Zhuochang Cai, Longqiang Shu, Chongyang Wang, Xuetao Xie, Xudong Liu","doi":"10.1016/j.arthro.2024.09.021","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>To explore the potential of M2 macrophage-derived exosomes (M2-Exos) in enhancing tendon-to-bone healing in aged rats by mitigating cellular senescence of bone marrow-derived stem cells (BMSCs).</p><p><strong>Methods: </strong>In vitro, the effects of M2-Exos on alleviating cellular senescence and improving chondrogenic potential of senescent BMSCs were evaluated. Rats (24 young and 48 aged) with chronic rotator cuff tear (RCT) were repaired and assigned into 3 groups: young group (young rats injected with fibrin at the enthesis), aged group (aged rats injected with fibrin at the enthesis), and aged + M2-Exos group (aged rats injected with fibrin containing M2-Exos at the enthesis). At 6 and 12 weeks after repair, enthesis regeneration was evaluated. Proteomic analysis was conducted to explore the mechanism through which M2-Exos mitigated cellular senescence.</p><p><strong>Results: </strong>In senescent BMSCs treated with M2-Exos, there was a reduction in senescence biomarkers including senescence-associated β-galactosidase, p53, p21, and senescence-associated secretory phenotype (P < .001). M2-Exos also enhanced chondrogenic potential of senescent BMSCs, reflected in greater Bern score (P < .001) and increased expression of Sox9 (P = .013), Col2a1 (P < .001), and Acan (P < .001). Histologically, aged rats treated with M2-Exos demonstrated significantly greater histologic scores (P < .001 at both 6 and 12 weeks) and increased fibrocartilage regeneration at the enthesis. Biomechanically, these rats exhibited greater failure load, stiffness, and stress (all P < .001) at 12 weeks. Mechanistically, proteomic analysis suggested that M2-Exos might alleviate cellular senescence by potentially regulating DNA replication and repair.</p><p><strong>Conclusions: </strong>M2-Exos can significantly alleviate BMSC senescence and thereby enhance tendon-to-bone healing in an aged rat RCT model.</p><p><strong>Clinical relevance: </strong>This study suggests the potential utility of M2-Exos as a therapy for RCT in the older population.</p>","PeriodicalId":55459,"journal":{"name":"Arthroscopy-The Journal of Arthroscopic and Related Surgery","volume":null,"pages":null},"PeriodicalIF":4.4000,"publicationDate":"2024-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Arthroscopy-The Journal of Arthroscopic and Related Surgery","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.arthro.2024.09.021","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ORTHOPEDICS","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose: To explore the potential of M2 macrophage-derived exosomes (M2-Exos) in enhancing tendon-to-bone healing in aged rats by mitigating cellular senescence of bone marrow-derived stem cells (BMSCs).

Methods: In vitro, the effects of M2-Exos on alleviating cellular senescence and improving chondrogenic potential of senescent BMSCs were evaluated. Rats (24 young and 48 aged) with chronic rotator cuff tear (RCT) were repaired and assigned into 3 groups: young group (young rats injected with fibrin at the enthesis), aged group (aged rats injected with fibrin at the enthesis), and aged + M2-Exos group (aged rats injected with fibrin containing M2-Exos at the enthesis). At 6 and 12 weeks after repair, enthesis regeneration was evaluated. Proteomic analysis was conducted to explore the mechanism through which M2-Exos mitigated cellular senescence.

Results: In senescent BMSCs treated with M2-Exos, there was a reduction in senescence biomarkers including senescence-associated β-galactosidase, p53, p21, and senescence-associated secretory phenotype (P < .001). M2-Exos also enhanced chondrogenic potential of senescent BMSCs, reflected in greater Bern score (P < .001) and increased expression of Sox9 (P = .013), Col2a1 (P < .001), and Acan (P < .001). Histologically, aged rats treated with M2-Exos demonstrated significantly greater histologic scores (P < .001 at both 6 and 12 weeks) and increased fibrocartilage regeneration at the enthesis. Biomechanically, these rats exhibited greater failure load, stiffness, and stress (all P < .001) at 12 weeks. Mechanistically, proteomic analysis suggested that M2-Exos might alleviate cellular senescence by potentially regulating DNA replication and repair.

Conclusions: M2-Exos can significantly alleviate BMSC senescence and thereby enhance tendon-to-bone healing in an aged rat RCT model.

Clinical relevance: This study suggests the potential utility of M2-Exos as a therapy for RCT in the older population.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
M2巨噬细胞衍生的外泌体通过缓解老龄大鼠的细胞衰老促进肌腱到骨的愈合。
目的:探讨M2巨噬细胞衍生的外泌体(M2-Exos)通过减轻骨髓干细胞(BMSCs)的细胞衰老来促进老年大鼠肌腱到骨愈合的潜力:方法:在体外评估了M2-Exos对缓解细胞衰老和提高衰老骨髓干细胞软骨生成潜能的作用。对二十四只年轻和四十八只老年慢性肩袖撕裂(RCT)大鼠进行修复,并将其分为三组:年轻组(年轻大鼠在关节内注射纤维蛋白)、老年组(老年大鼠在关节内注射纤维蛋白)和老年 + M2-Exos 组(老年大鼠在关节内注射含有 M2-Exos 的纤维蛋白)。修复六周和十二周后,对假体再生进行评估。为探索M2-Exos缓解细胞衰老的机制,进行了蛋白质组学分析:结果:经 M2-Exos 处理的衰老 BMSCs 中,衰老生物标志物减少,包括衰老相关的 β-半乳糖苷酶、p53、p21 和衰老相关的分泌表型(P < .001)。M2-Exos 还增强了衰老 BMSCs 的软骨潜能,这体现在 Bern 评分提高(P < .001)和 Sox9(P = .013)、Col2a1(P < .001)和 Acan(P < .001)的表达增加。从组织学角度来看,接受 M2-Exos 治疗的老龄大鼠的组织学评分明显更高(6 周和 12 周时的评分均低于 0.001),且内关节处的纤维软骨再生增加。在生物力学方面,这些大鼠在 12 周时表现出更大的失效负荷、硬度和应力(所有 P < .001)。从机理上讲,蛋白质组分析表明,M2-Exos可能通过调节DNA复制和修复来缓解细胞衰老:结论:M2-Exos 能明显缓解 BMSC 的衰老,从而促进老龄大鼠 RCT 模型中肌腱到骨的愈合:这项研究表明,M2-Exos 可用于治疗老年人的 RCT。
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 去求助
来源期刊
CiteScore
9.30
自引率
17.00%
发文量
555
审稿时长
58 days
期刊介绍: Nowhere is minimally invasive surgery explained better than in Arthroscopy, the leading peer-reviewed journal in the field. Every issue enables you to put into perspective the usefulness of the various emerging arthroscopic techniques. The advantages and disadvantages of these methods -- along with their applications in various situations -- are discussed in relation to their efficiency, efficacy and cost benefit. As a special incentive, paid subscribers also receive access to the journal expanded website.
期刊最新文献
Author Reply to Editorial Comment "Autologous Minced Repair of Knee Cartilage Is Safely and Effectively Performed Using Arthroscopic Techniques". Culture Expansion Alters Human Bone Marrow Derived Mesenchymal Stem Cell Production of Osteoarthritis-relevant Cytokines and Growth Factors. Steeper Slope of the Medial Tibial Plateau, Greater Varus Alignment, and Narrower Intercondylar Distance and Notch Width Increase Risk for Medial Meniscus Posterior Root Tears: A Systematic Review. Synthetic Medial Meniscus Implant Demonstrates High Reoperation Rates: Patients Who Retain Implant or Require Implant Exchange SHow Improvement For Post Meniscectomy Knee Pain Is Associated With Clinical Improvement But High Reoperation Rates At 2-Years Post-Operatively. The Knee Anterolateral Ligament is Present in 82% of North American and 65% of European But Only in 46% of Asian Studies: A Systematic Review of Frequency and Anatomy.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1