Sustained release of ubiquitin-like protein ISG-15 enhances tendon-to-bone healing following anterior cruciate ligament reconstruction in a mouse model.

IF 4.8 3区 工程技术 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Frontiers in Bioengineering and Biotechnology Pub Date : 2025-03-12 eCollection Date: 2025-01-01 DOI:10.3389/fbioe.2025.1550584
Jun-Cheng Yao, Jie-Xin Zhang, Xuan Wang, Yu-Hao Wu, Hao-Lin Ke, Jia-Rong Liang, Yan Shao, Jin-Tao Li, Yuan Liu, Dao-Zhang Cai, Jian-Ying Pan
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Abstract

The process of tendon-to-bone healing is regulated by several proteins and cytokines that play critical roles in shaping biomechanical properties and functional recovery. Among these, the ubiquitin-like protein ISG-15 has been reported to have a beneficial effect on tissue repair. However, its specific function in tendon-to-bone interface regeneration has not been well characterized. This study investigated the function of ISG15 in vitro and addressed its in vivo effects on tendon and bone healing. In this study, wild-type C57/BL6 mice underwent anterior cruciate ligament (ACL) reconstruction surgery, with a sustained-release hydrogel containing ISG15 protein injected into the bone tunnels in the treatment group. To assess its therapeutic potential, bone-tendon interface growth was evaluated through histological staining, while micro-computed tomography (Micro-CT) was employed to quantify newly formed bone and bone density within the bone tunnels. Additionally, biomechanical testing was performed to measure the mechanical strength of the grafted tendons, and immunohistochemistry was conducted to detect the expression of Runx2 and osteocalcin (OCN) at the bone-tendon interface. In vitro results showed that an appropriate concentration of ISG-15 has the ability to promote osteogenic differentiation of bone marrow mesenchymal stem cells. Also, In the in vivo experiments, the local application of ISG15 protein significantly reduced inflammatory tissue growth during the early stages of healing and minimized bone resorption in the later stages. Furthermore, Micro-CT analysis showed an increased volume of newly formed bone in the treatment group, while biomechanical testing demonstrated enhanced mechanical strength of the grafted tendons. In summary, this study suggests that the localized sustained release of ISG15 protein during ACL reconstruction facilitates tendon-to-bone interface repair by promoting bone ingrowth, ultimately leading to improved biomechanical properties and functional recovery.

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在小鼠模型中,持续释放泛素样蛋白ISG-15促进前交叉韧带重建后肌腱到骨的愈合。
肌腱到骨的愈合过程受几种蛋白质和细胞因子的调控,这些蛋白质和细胞因子在形成生物力学特性和功能恢复中起着关键作用。其中,泛素样蛋白ISG-15已被报道对组织修复有有益作用。然而,其在肌腱-骨界面再生中的具体功能尚未得到很好的表征。本研究在体外研究了ISG15的功能,并探讨了其在体内对肌腱和骨愈合的影响。在本研究中,野生型C57/BL6小鼠接受前交叉韧带(ACL)重建手术,治疗组在骨隧道内注射含有ISG15蛋白的缓释水凝胶。为了评估其治疗潜力,通过组织学染色评估骨-肌腱界面生长情况,同时采用显微计算机断层扫描(Micro-CT)量化骨隧道内新形成的骨和骨密度。此外,通过生物力学测试测量移植肌腱的机械强度,并通过免疫组化检测Runx2和骨钙素(OCN)在骨-肌腱界面的表达。体外实验结果表明,适当浓度的ISG-15具有促进骨髓间充质干细胞成骨分化的能力。此外,在体内实验中,局部应用ISG15蛋白可显著减少早期愈合阶段的炎症组织生长,减少后期骨吸收。此外,Micro-CT分析显示治疗组新生骨体积增加,而生物力学测试显示移植肌腱的机械强度增强。综上所述,本研究表明,在ACL重建过程中,ISG15蛋白的局部持续释放通过促进骨向内生长来促进肌腱-骨界面修复,最终改善生物力学性能和功能恢复。
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来源期刊
Frontiers in Bioengineering and Biotechnology
Frontiers in Bioengineering and Biotechnology Chemical Engineering-Bioengineering
CiteScore
8.30
自引率
5.30%
发文量
2270
审稿时长
12 weeks
期刊介绍: The translation of new discoveries in medicine to clinical routine has never been easy. During the second half of the last century, thanks to the progress in chemistry, biochemistry and pharmacology, we have seen the development and the application of a large number of drugs and devices aimed at the treatment of symptoms, blocking unwanted pathways and, in the case of infectious diseases, fighting the micro-organisms responsible. However, we are facing, today, a dramatic change in the therapeutic approach to pathologies and diseases. Indeed, the challenge of the present and the next decade is to fully restore the physiological status of the diseased organism and to completely regenerate tissue and organs when they are so seriously affected that treatments cannot be limited to the repression of symptoms or to the repair of damage. This is being made possible thanks to the major developments made in basic cell and molecular biology, including stem cell science, growth factor delivery, gene isolation and transfection, the advances in bioengineering and nanotechnology, including development of new biomaterials, biofabrication technologies and use of bioreactors, and the big improvements in diagnostic tools and imaging of cells, tissues and organs. In today`s world, an enhancement of communication between multidisciplinary experts, together with the promotion of joint projects and close collaborations among scientists, engineers, industry people, regulatory agencies and physicians are absolute requirements for the success of any attempt to develop and clinically apply a new biological therapy or an innovative device involving the collective use of biomaterials, cells and/or bioactive molecules. “Frontiers in Bioengineering and Biotechnology” aspires to be a forum for all people involved in the process by bridging the gap too often existing between a discovery in the basic sciences and its clinical application.
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