用于慢性鼓膜穿孔治疗的潜伏干细胞刺激径向排列电纺纳米纤维贴片

Juo Lee, Sangbae Park, Beomyong Shin, Yeon Ju Kim, Sungmin Lee, Jungsil Kim, Kyoung-Je Jang, Oak-Sung Choo, Jangho Kim, Hoon Seonwoo, Jong Hoon Chung, Yun-Hoon Choung
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引用次数: 0

摘要

慢性鼓膜(TM)穿孔是一种由外伤或炎症引起的鼓室疾病。最近的一项研究表明,通过应用具有径向排列纳米结构的纳米纤维和控制释放生长因子,在促进慢性鼓膜穿孔再生方面取得了重大进展。然而,含有干细胞刺激因子的径向排列纳米结构却从未使用过。本研究开发了胰岛素样生长因子结合因子2(IGFBP2)融入径向排列纳米纤维贴片(IRA-NFPs),并将其应用于慢性TM穿孔的再生。IRA-NFPs 是通过在三氟乙醇和醋酸(9:1)中电纺 8 wt% 聚己内酯制备而成。使用平板和定制的圆形收集器分别成功制备了随机纳米纤维(RF)和排列纳米纤维(AF)。傅立叶变换红外光谱证实了 IGFBP2 的存在,而且 IGFBP2 的释放可持续长达 20 天。体外研究显示,与 RF 相比,AF 上的细胞增殖和迁移能力更强,IGFBP2 的加入进一步促进了这些效果。定量实时 PCR 显示 mRNA 下调,这与迁移加速和细胞融合度增加有关。使用 Choung's COM 模型 1 进行的体内研究显示,与对照组相比,IGFBP2-负载的 RF 和 AF 补丁分别将再生成功率提高了 1.59 倍和 2.23 倍,同时将愈合时间缩短了 2.5 倍。此外,IGFBP2-纳入的AF在愈合较大穿孔方面表现出卓越的疗效,组织学上与原生TM的相似性更高。这项研究结合了干细胞刺激因子和排列的纳米结构,提出了一种新方法,有可能取代传统的手术方法,用于慢性颞叶穿孔的再生。意义声明:由于炎症、供血不足和缺乏生长因子,慢性中耳炎(COM)影响着全球约2亿人。目前的手术疗法存在成本高、麻醉风险大等局限性。最近的研究探索了使用具有径向排列纳米结构和生长因子可控释放的纳米纤维来治疗慢性鼓膜(TM)穿孔。本研究开发了胰岛素样生长因子结合蛋白 2(IGFBP2)融入径向排列纳米纤维贴片(IRA-NFPs),并将其用于慢性鼓膜穿孔的再生。我们通过体外和体内研究评估了它们的特性和功效。IRA-NFPs在慢性颞叶穿孔模型中显示出良好的愈合能力。这种创新方法有望改善 COM 管理、降低手术成本并提高患者安全性。
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Latent stem cell-stimulating radially aligned electrospun nanofibrous patches for chronic tympanic membrane perforation therapy.

Chronic tympanic membrane (TM) perforation is a tubotympanic disease caused by either traumatic injury or inflammation. A recent study demonstrated significant progress in promoting the regeneration of chronic TM perforations through the application of nanofibers with radially aligned nanostructures and controlled release of growth factors. However, radially aligned nanostructures with stem cell-stimulating factors have never been used. In this study, insulin-like growth factor binding factor 2 (IGFBP2)-incorporated radially aligned nanofibrous patches (IRA-NFPs) were developed and applied to regenerate chronic TM perforations. The IRA-NFPs were prepared by electrospinning 8 wt% polycaprolactone in trifluoroethanol and acetic acid (9:1). Random nanofibers (RFs) and aligned nanofibers (AFs) were successfully fabricated using a flat plate and a custom-designed circular collector, respectively. The presence of IGFBP2 was confirmed via Fourier transform infrared spectroscopy and the release of IGFBP2 was sustained for up to 20 days. In vitro studies revealed enhanced cellular proliferation and migration on AFs compared to RFs, and the incorporation of IGFBP2 further promoted these effects. Quantitative real-time PCR revealed mRNA downregulation, correlating with accelerated migration and increased cell confluency. In vivo studies showed IGFBP2-loaded RF and AF patches increased regeneration success rates by 1.59-fold and 2.23-fold, respectively, while also reducing healing time by 2.5-fold compared to the control. Furthermore, IGFBP2-incorporated AFs demonstrated superior efficacy in healing larger perforations with enhanced histological similarity to native TMs. This study, combining stem cell stimulating factors and aligned nanostructures, proposes a novel approach potentially replacing conventional surgical methods for chronic TM perforation regeneration. STATEMENT OF SIGNIFICANCE: Chronic otitis media (COM) affects approximately 200 million people worldwide due to inflammation, inadequate blood supply, and lack of growth factors. Current surgical treatments have limitations like high costs and anesthetic risks. Recent research explored the use of nanofibers with radially aligned nanostructures and controlled release of growth factors to treat chronic tympanic membrane (TM) perforations. In this study, insulin-like growth factor binding protein 2 (IGFBP2)-incorporated radially aligned nanofibrous patches (IRA-NFPs) were developed and applied to regenerate chronic TM perforations. We assessed their properties and efficacy through in vitro and in vivo studies. IRA-NFPs showed promising healing capabilities with chronic TM perforation models. This innovative approach has the potential to improve COM management, reduce surgery costs, and enhance patient safety.

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