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胶原蛋白支架上的CBD共轭BMP抑制外泌体用于双靶点跟腱修复:协同再生与预防异位骨化

CBD-conjugated BMP-inhibiting exosomes on collagen scaffold dual-target Achilles tendon repair: Synergistic regeneration and heterotopic ossification prevention.

作者信息

Xu Yan, Huang Jiaqiang, Mai Yingjie, Zhang Zhiyuan, Li Siqi, Lin Haofeng, Wei Fuxin, Chen Yang

机构信息

Department of Orthopaedics, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China.

Shenzhen Key Laboratory of Bone Tissue Repair and Translational Research, China.

出版信息

Mater Today Bio. 2025 Apr 22;32:101790. doi: 10.1016/j.mtbio.2025.101790. eCollection 2025 Jun.

Abstract

Tendon injuries in the aging population are often complicated by heterotopic ossification (HO), hindering functional recovery. Exosomes from tendon stem/progenitor cells (TSPCs) promote regeneration but may also induce osteogenesis, contributing to HO. Preconditioning with the BMP inhibitor LDN193189 and modification with collagen-binding peptides (CBD) can enhance the tenogenic potential of exosomes while mitigating osteogenic effects. We evaluated the efficacy of a 3D-printed scaffold loaded with LDN-preconditioned, CBD-modified exosomes (3D-CBD@LDN/Exos) derived from CD26 TSPCs in promoting Achilles tendon repair and preventing HO in aged Sprague-Dawley rats. CD26 TSPCs were isolated from rat tendons, and exosomes were collected after LDN treatment and subsequently modified with CBD. A scaffold composed of PLGA and collagen I was fabricated via 3D printing and loaded with the exosomes. Rats (20 months old) with 6-mm Achilles tendon defects were randomly assigned to Control, 3D-Exos, 3D-LDN/Exos, or 3D-CBD@LDN/Exos groups, and tendon regeneration was evaluated at 4 and 12 weeks using histology, ECM quantification, micro-CT, and biomechanical testing. At 12 weeks, the 3D-CBD@LDN/Exos group exhibited near-normal histology, enhanced collagen and sGAG deposition, biomechanical properties comparable to native tendons, and significantly reduced HO, indicating that this dual-targeted strategy holds promise for tendon repair.

摘要

老年人群的肌腱损伤常因异位骨化(HO)而复杂化,阻碍功能恢复。来自肌腱干/祖细胞(TSPCs)的外泌体可促进再生,但也可能诱导成骨,导致异位骨化。用骨形态发生蛋白(BMP)抑制剂LDN193189预处理并结合胶原蛋白结合肽(CBD)进行修饰,可以增强外泌体的成腱潜力,同时减轻成骨作用。我们评估了一种3D打印支架的疗效,该支架负载了来自CD26 TSPCs的经LDN预处理、CBD修饰的外泌体(3D-CBD@LDN/Exos),用于促进老年Sprague-Dawley大鼠的跟腱修复并预防异位骨化。从大鼠肌腱中分离出CD26 TSPCs,经LDN处理后收集外泌体,随后用CBD进行修饰。通过3D打印制备了一种由聚乳酸-羟基乙酸共聚物(PLGA)和I型胶原蛋白组成的支架,并负载外泌体。将有6毫米跟腱缺损的20月龄大鼠随机分为对照组、3D-Exos组、3D-LDN/Exos组或3D-CBD@LDN/Exos组,并在4周和12周时使用组织学、细胞外基质(ECM)定量、微型计算机断层扫描(micro-CT)和生物力学测试评估肌腱再生情况。在12周时,3D-CBD@LDN/Exos组表现出接近正常的组织学特征,胶原蛋白和硫酸糖胺聚糖(sGAG)沉积增加,生物力学性能与天然肌腱相当,且异位骨化明显减少,表明这种双靶点策略在肌腱修复方面具有前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c01e/12059345/60d0b891be47/ga1.jpg

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