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泛素样蛋白ISG-15的持续释放增强了小鼠前交叉韧带重建术后的腱骨愈合。

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

作者信息

Yao Jun-Cheng, Zhang Jie-Xin, Wang Xuan, Wu Yu-Hao, Ke Hao-Lin, Liang Jia-Rong, Shao Yan, Li Jin-Tao, Liu Yuan, Cai Dao-Zhang, Pan Jian-Ying

机构信息

Department of Joint Surgery, Center for Orthopaedic Surgery, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China.

Department of Orthopedics, Orthopedic Hospital of Guangdong Province, Academy of Orthopedics·Guangdong Province, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China.

出版信息

Front Bioeng Biotechnol. 2025 Mar 12;13:1550584. doi: 10.3389/fbioe.2025.1550584. eCollection 2025.

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 and addressed its 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. 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 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.

摘要

肌腱与骨愈合的过程受多种蛋白质和细胞因子的调节,这些蛋白质和细胞因子在塑造生物力学特性和功能恢复方面发挥着关键作用。其中,泛素样蛋白ISG-15已被报道对组织修复具有有益作用。然而,其在肌腱与骨界面再生中的具体功能尚未得到充分阐明。本研究调查了ISG15的功能,并探讨了其对肌腱和骨愈合的影响。在本研究中,野生型C57/BL6小鼠接受了前交叉韧带(ACL)重建手术,治疗组将含有ISG15蛋白的缓释水凝胶注入骨隧道。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,同时采用微型计算机断层扫描(Micro-CT)对骨隧道内新形成的骨和骨密度进行量化。此外,进行生物力学测试以测量移植肌腱的机械强度,并进行免疫组织化学检测骨-肌腱界面处Runx2和骨钙素(OCN)的表达。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,在实验中,局部应用ISG15蛋白可在愈合早期显著减少炎性组织生长,并在后期将骨吸收降至最低。此外,Micro-CT分析显示治疗组新形成的骨体积增加,而生物力学测试表明移植肌腱的机械强度增强。总之,本研究表明,在ACL重建过程中局部持续释放ISG15蛋白可通过促进骨长入来促进肌腱与骨界面修复,最终改善生物力学特性和功能恢复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2d2/11937028/e95c1548c547/fbioe-13-1550584-g001.jpg

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