Wu Xiang-Dong, Kang Lin, Tian Jingjing, Wu Yuanhao, Huang Yue, Liu Jieying, Wang Hai, Qiu Guixing, Wu Zhihong
Department of Orthopaedic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100730, China.
Medical Science Research Center (MRC), Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100730, China.
Mater Today Bio. 2022 Jun 11;15:100319. doi: 10.1016/j.mtbio.2022.100319. eCollection 2022 Jun.
Graft healing after anterior cruciate ligament reconstruction (ACLR) involves slow biological processes, and various types of biological modulations have been explored to promote tendon-to-bone integration. Exosomes have been extensively studied as a promising new cell-free strategy for tissue regeneration, but few studies have reported their potential in tendon-to-bone healing. In this study, a novel type of exosome derived from magnetically actuated (iron oxide nanoparticles (IONPs) combined with a magnetic field) bone mesenchymal stem cells (BMSCs) (IONP-Exos) was developed, and the primary purpose of this study was to determine whether IONP-Exos exert more significant effects on tendon-to-bone healing than normal BMSC-derived exosomes (BMSC-Exos). Here, we isolated and characterized the two types of exosomes, conducted in vitro experiments to measure their effects on fibroblasts (NIH3T3), and performed in vivo experiments to compare the effects on tendon-to-bone integration. Moreover, functional exploration of exosomal miRNAs was further performed by utilizing a series of gain- and loss-of-function experiments. Experimental results showed that both BMSC-Exos and IONP-Exos could be shuttled intercellularly into NIH3T3 fibroblasts and enhanced fibroblast activity, including proliferation, migration, and fibrogenesis. In vivo, we found that IONP-Exos significantly prevented peri-tunnel bone loss, promoted more osseous ingrowth into the tendon graft, increased fibrocartilage formation at the tendon-bone tunnel interface, and induced a higher maximum load to failure than BMSC-Exos. Furthermore, overexpression of miR-21-5p remarkably enhanced fibrogenesis in vitro, and SMAD7 was shown to be involved in the promotive effect of IONP-Exos on tendon-to-bone healing. Our findings may provide new insights into the regulatory roles of IONPs in IONP-Exos communication via stimulating exosomal miR-21-5p secretion and the SMAD7 signaling pathway in the fibrogenic process of tendon-to-bone integration. This work could provide a new strategy to promote tendon-to-bone healing for tissue engineering in the future.
前交叉韧带重建(ACLR)后的移植物愈合涉及缓慢的生物学过程,人们已经探索了各种类型的生物调节方法来促进腱骨整合。外泌体作为一种有前景的新型无细胞组织再生策略已得到广泛研究,但很少有研究报道其在腱骨愈合中的潜力。在本研究中,我们开发了一种新型的源自磁驱动(氧化铁纳米颗粒(IONPs)与磁场结合)的骨间充质干细胞(BMSCs)的外泌体(IONP-Exos),本研究的主要目的是确定IONP-Exos对腱骨愈合的影响是否比正常BMSC来源的外泌体(BMSC-Exos)更显著。在此,我们分离并表征了这两种类型的外泌体,进行体外实验以测量它们对成纤维细胞(NIH3T3)的影响,并进行体内实验以比较它们对腱骨整合的影响。此外,通过一系列功能获得和功能丧失实验对外泌体miRNAs进行了进一步的功能探索。实验结果表明,BMSC-Exos和IONP-Exos均可在细胞间穿梭进入NIH3T3成纤维细胞并增强成纤维细胞活性,包括增殖、迁移和纤维化。在体内,我们发现IONP-Exos显著预防了隧道周围骨质流失,促进更多骨长入肌腱移植物,增加了腱骨隧道界面处的纤维软骨形成,并诱导了比BMSC-Exos更高的最大破坏载荷。此外,miR-21-5p的过表达在体外显著增强了纤维化,并且SMAD7被证明参与了IONP-Exos对腱骨愈合的促进作用。我们的研究结果可能为IONPs在IONP-Exos通讯中的调节作用提供新的见解,即通过刺激外泌体miR-21-5p分泌和SMAD7信号通路参与腱骨整合的纤维化过程。这项工作可为未来组织工程促进腱骨愈合提供一种新策略。