血小板裂解液功能化甲基丙烯酸明胶微球促进牙髓再生血管生成

IF 9.4 1区 医学 Q1 ENGINEERING, BIOMEDICAL
Qingyuan Zhang , Ting Yang , Ruitao Zhang , Xi Liang , Ge Wang , Yuan Tian , Li Xie , Weidong Tian
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引用次数: 21

摘要

快速血管生成是牙髓再生的挑战之一。近年来,装载促血管生成生长因子(GFs)的聚合物微球系统在促进牙髓再生血管化方面有很大的前景。此外,多种GFs的协同效应被认为更有利,但它们的联合使用相当复杂和昂贵。在这里,我们的目的是将人类血小板裂解液(PL),一种天然衍生的多种血小板池,纳入明胶甲基丙烯酸酯(GelMA)微球系统(GP)中,该系统被拉脱石(GPL)进一步修饰,拉脱石(GPL)是一种具有高效给药能力的纳米粘土。利用静电微滴技术成功制备了这些尺寸范围为180 ~ 380µm的杂化微球。与GelMA掺入PL和Laponite后,杂化水凝胶的杨氏模量提高了约3倍,溶胀率和降解率同时降低。pl衍生的GFs从GP和GPL微球中持续释放长达28天,而后者释放相对较慢。此外,释放的GFs还能有效诱导人脐内皮细胞(HUVECs)形成小管,促进人牙髓干细胞(hDPSCs)迁移。此外,GelMA微球中的PL成分显著改善了包被的hdpsc的增殖、扩散和牙源性分化。皮下植入结果进一步证实,GP和GPL组均能促进微血管形成和髓样组织再生。本研究表明,结合pl的GelMA微球系统是一种很有前途的促进血管化牙髓再生的功能载体。载促血管生成生长因子(GFs)的聚合物微球系统在血管化牙髓再生中具有广阔的应用前景。本研究采用静电微滴法制备了一种包含人血小板裂解液(PL)和纳米粘土拉脱石的功能凝胶微球体系。结果表明,与纯GelMA微球相比,GelMA/PL/Laponite微球可显著改善包被hdpsc的扩散、增殖和牙源性分化。此外,它们还能促进体内微血管的形成和髓样组织的再生。这种混合微球系统在促进再生牙髓和其他组织的微血管形成方面具有很大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Platelet lysate functionalized gelatin methacrylate microspheres for improving angiogenesis in endodontic regeneration

Platelet lysate functionalized gelatin methacrylate microspheres for improving angiogenesis in endodontic regeneration

Rapid angiogenesis is one of the challenges in endodontic regeneration. Recently, tailored polymeric microsphere system that loaded pro-angiogenic growth factors (GFs) is promising in facilitating vascularization in dental pulp regeneration. In addition, the synergistic effect of multiple GFs is considered more beneficial, but combination usage of them is rather complex and costly. Herein, we aimed to incorporate human platelet lysate (PL), a natural-derived pool of multiple GFs, into gelatin methacrylate (GelMA) microsphere system (GP), which was further modified by Laponite (GPL), a nanoclay with efficient drug delivery ability. These hybrid microspheres were successfully fabricated by electrostatic microdroplet technique with suitable size range (180∼380 µm). After incorporation of the PL and Laponite with GelMA, the Young's modulus of the hybrid hydrogel increased up to about 3-fold and the swelling and degradation rate decreased simultaneously. The PL-derived GFs continued to release up to 28 days from both the GP and GPL microspheres, while the latter released relatively more slowly. What's more, the released GFs could effectively induce tubule formation of human umbilical endothelial cells (HUVECs) and also promote human dental pulp stem cells (hDPSCs) migration. Additionally, the PL component in the GelMA microspheres significantly improved the proliferation, spreading, and odontogenic differentiation of the encapsulated hDPSCs. As further verified by the subcutaneous implantation results, both of the GP and GPL groups enhanced microvascular formation and pulp-like tissue regeneration. This work demonstrated that PL-incorporating GelMA microsphere system was a promising functional vehicle for promoting vascularized endodontic regeneration.

Statement of significance

Polymeric microsphere system loaded with pro-angiogenic growth factors (GFs) shows great promise for regeneration of vascularized dental pulp. Herein, we prepared a functional GelMA microsphere system incorporated with human platelet lysates (PL) and nanoclay Laponite by the electrostatic microdroplet method. The results demonstrated that the GelMA/PL/Laponite microspheres significantly improved the spreading, proliferation, and odontogenic differentiation of the encapsulated hDPSCs compared with pure GelMA microspheres. Moreover, they also enhanced microvascular formation and pulp-like tissue regeneration in vivo. This hybrid microsphere system has great potential to accelerate microvessel formation in regenerated dental pulp and other tissues.

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来源期刊
Acta Biomaterialia
Acta Biomaterialia 工程技术-材料科学:生物材料
CiteScore
16.80
自引率
3.10%
发文量
776
审稿时长
30 days
期刊介绍: Acta Biomaterialia is a monthly peer-reviewed scientific journal published by Elsevier. The journal was established in January 2005. The editor-in-chief is W.R. Wagner (University of Pittsburgh). The journal covers research in biomaterials science, including the interrelationship of biomaterial structure and function from macroscale to nanoscale. Topical coverage includes biomedical and biocompatible materials.
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