Kevin J M Paulussen, Christopher M T Hayden, Taylor Griffin, Keith Baar
{"title":"Exosome enriched serum enhances engineered ligament mechanics and collagen content with no additional benefit of resistance exercise.","authors":"Kevin J M Paulussen, Christopher M T Hayden, Taylor Griffin, Keith Baar","doi":"10.1016/j.mbplus.2025.100181","DOIUrl":null,"url":null,"abstract":"<p><p>Following resistance exercise, systemic changes foster improved functionality of tendons and ligaments. Post-exercise, muscle tissue releases exosomes that are thought to facilitate inter-tissue communication. To determine the potential role of exosomes in the exercise-induced adaptations of tendons and ligaments, we modified our engineered human ligament (EHL) model to work with exosome-enriched serum. Treatment of the EHLs with exosomes enriched from fetal bovine serum (fbEXO) resulted in enhanced ligament mechanics and increased collagen content in a dose-response fashion (maximum tensile load [MTL]: 10 %: 0.196 ± 0.138 N, 20 %: 0.278 ± 0.103 N, 40 %: 0.840 ± 0.092 N; r<sup>2</sup> = 0.858, <i>P</i> < 0.0001; collagen content: 10 %: 1.073 ± 12.49 µg, 20 %: 86.43 ± 71.65 µg, 40 %: 145.7 ± 84.11 µg; r<sup>2</sup> = 0.4735, <i>P</i> = 0.0046). After optimizing an exosome enriched feeding protocol using fbEXO, we confirmed that exosomes enriched from human serum (hsEXO) could sustain EHL function. Subsequently, twelve healthy, recreationally active volunteers (22 ± 3 y, 1,68 ± 0.10 m, 65.6 ± 27.8 kg; 6F/6M) performed a single bout of resistance exercise. Serum samples were collected prior to and 15 min post-exercise, and exosomes were enriched from these samples for treatment of EHLs. EHL function and collagen content did not differ when treated with hsEXO obtained at rest or post-resistance exercise (MTL: 1.30 ± 0.36 vs. 1.20 ± 0.36 N, <i>P</i> = 0.3950; collagen content: 424.6 ± 47.68 vs. 425.2 ± 44.46 µg, <i>P</i> = 0.9663). This model provides a novel way to determine the role of exosomes in connective tissue development and adaptation. The identification of circulating exercise factors that enhance tendon and ligament function remains to be fully elucidated.</p>","PeriodicalId":52317,"journal":{"name":"Matrix Biology Plus","volume":"27 ","pages":"100181"},"PeriodicalIF":0.0000,"publicationDate":"2025-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12357142/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Matrix Biology Plus","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.mbplus.2025.100181","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Following resistance exercise, systemic changes foster improved functionality of tendons and ligaments. Post-exercise, muscle tissue releases exosomes that are thought to facilitate inter-tissue communication. To determine the potential role of exosomes in the exercise-induced adaptations of tendons and ligaments, we modified our engineered human ligament (EHL) model to work with exosome-enriched serum. Treatment of the EHLs with exosomes enriched from fetal bovine serum (fbEXO) resulted in enhanced ligament mechanics and increased collagen content in a dose-response fashion (maximum tensile load [MTL]: 10 %: 0.196 ± 0.138 N, 20 %: 0.278 ± 0.103 N, 40 %: 0.840 ± 0.092 N; r2 = 0.858, P < 0.0001; collagen content: 10 %: 1.073 ± 12.49 µg, 20 %: 86.43 ± 71.65 µg, 40 %: 145.7 ± 84.11 µg; r2 = 0.4735, P = 0.0046). After optimizing an exosome enriched feeding protocol using fbEXO, we confirmed that exosomes enriched from human serum (hsEXO) could sustain EHL function. Subsequently, twelve healthy, recreationally active volunteers (22 ± 3 y, 1,68 ± 0.10 m, 65.6 ± 27.8 kg; 6F/6M) performed a single bout of resistance exercise. Serum samples were collected prior to and 15 min post-exercise, and exosomes were enriched from these samples for treatment of EHLs. EHL function and collagen content did not differ when treated with hsEXO obtained at rest or post-resistance exercise (MTL: 1.30 ± 0.36 vs. 1.20 ± 0.36 N, P = 0.3950; collagen content: 424.6 ± 47.68 vs. 425.2 ± 44.46 µg, P = 0.9663). This model provides a novel way to determine the role of exosomes in connective tissue development and adaptation. The identification of circulating exercise factors that enhance tendon and ligament function remains to be fully elucidated.
在抗阻运动之后,全身的变化促进了肌腱和韧带功能的改善。运动后,肌肉组织释放被认为促进组织间交流的外泌体。为了确定外泌体在运动诱导的肌腱和韧带适应性中的潜在作用,我们修改了我们的工程人韧带(EHL)模型,使其与外泌体富集的血清一起工作。胎牛血清富外泌体(fbEXO)处理EHLs后,韧带力学增强,胶原含量呈剂量-效应增加(最大拉伸载荷[MTL]: 10%: 0.196±0.138 N, 20%: 0.278±0.103 N, 40%: 0.840±0.092 N; r2 = 0.858, p2 = 0.4735, P = 0.0046)。在使用fbEXO优化了外泌体富集喂养方案后,我们证实了从人血清中富集的外泌体(hsEXO)可以维持EHL功能。随后,12名健康、娱乐活动的志愿者(22±3岁、1、68±0.10米、65.6±27.8公斤;6F/6M)进行单次阻力运动。在运动前和运动后15分钟收集血清样本,并从这些样本中富集外泌体用于治疗EHLs。静息或阻力运动后获得的hsEXO对EHL功能和胶原含量无显著影响(MTL: 1.30±0.36 vs 1.20±0.36 N, P = 0.3950;胶原含量:424.6±47.68 vs 425.2±44.46µg, P = 0.9663)。该模型为确定外泌体在结缔组织发育和适应中的作用提供了一种新的方法。增强肌腱和韧带功能的循环运动因子的鉴定仍有待充分阐明。