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磁性驱动的骨髓间充质干细胞来源的外泌体通过miR-21-5p/SMAD7途径促进肌腱-骨愈合。

Exosomes derived from magnetically actuated bone mesenchymal stem cells promote tendon-bone healing through the miR-21-5p/SMAD7 pathway.

作者信息

Wu Xiang-Dong, Kang Lin, Tian Jingjing, Wu Yuanhao, Huang Yue, Liu Jieying, Wang Hai, Qiu Guixing, Wu Zhihong

机构信息

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.

出版信息

Mater Today Bio. 2022 Jun 11;15:100319. doi: 10.1016/j.mtbio.2022.100319. eCollection 2022 Jun.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ad9/9218580/9a024295d6f0/ga1.jpg

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