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首页> 外文期刊>Acta biomaterialia >Enzymatic conjugation of a bioactive peptide into an injectable hyaluronic acid-tyramine hydrogel system to promote the formation of functional vasculature
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Enzymatic conjugation of a bioactive peptide into an injectable hyaluronic acid-tyramine hydrogel system to promote the formation of functional vasculature

机译:将生物活性肽酶促结合到可注射的透明质酸-酪胺水凝胶系统中,以促进功能性脉管系统的形成

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摘要

In this study, one-step enzyme-mediated preparation of a multi-functional injectable hyaluronic-acid-based hydrogel system is reported. Hydrogel was formed through the in situ coupling of phenol moieties by horseradish peroxidase (HRP) and hydrogen peroxide (H2O2), and bioactive peptides were simultaneously conjugated into the hydrogel during the gel formation process. The preparation of this multi-functional hydrogel was made possible by synthesizing peptides containing phenols which could couple with the phenol moieties of hyaluronic-acid-tyramine (HA-Tyr) during the HRP-mediated crosslinking reaction. Preliminary studies demonstrated that two phenol moieties per molecule resulted in a consistently high degree of conjugation into the HA-Tyr hydrogel network, unlike the one modified with one phenol moiety per molecule. Therefore, an Arg-Gly-Asp (RGD) peptide bearing two phenol moieties (phenol2-poly(ethylene glycol)-RGD) was designed for conjugation to endow the HA-Tyr hydrogel with adhesion signals and enhance its bioactivities. Human umbilical vein endothelial cells (HUVECs) cultured on or within the RGD-modified hydrogels showed significantly different adhesion behavior, from non-adherence on the HA-Tyr hydrogel to strong adhesion on hydrogels modified with phenol2-poly(ethylene glycol)-RGD. This altered cell adhesion behavior led to improved cell proliferation, migration and formation of capillary-like network in the hydrogel in vitro. More importantly, when HUVECs and human fibroblasts (HFF1) were encapsulated together in the RGD-modified HA-Tyr hydrogel, functional vasculature was observed inside the cell-laden gel after 2 weeks in the subcutaneous tissue. Taken together, the in situ conjugation of phenol2-poly(ethylene glycol)-RGD into HA-Tyr hydrogel system, coupled with the ease of incorporating cells, offers a simple and effective means to introduce biological signals for preparation of multi-functional injectable hydrogels for tissue engineering application.
机译:在这项研究中,报告了多功能可注射的透明质酸基水凝胶体系的一步酶介导制备。辣根过氧化物酶(HRP)和过氧化氢(H2O2)通过苯酚部分的原位偶联形成水凝胶,并且在凝胶形成过程中将生物活性肽同时偶联到水凝胶中。通过合成含有酚的肽,可以制备这种多功能水凝胶,在HRP介导的交联反应中,该肽可以与透明质酸-酪胺(HA-Tyr)的酚部分偶联。初步研究表明,每个分子中两个酚部分导致与HA-Tyr水凝胶网络的结合程度始终很高,这与每个分子中一个酚部分进行了修饰不同。因此,设计了带有两个酚部分的Arg-Gly-Asp(RGD)肽(酚2-聚(乙二醇)-RGD)进行缀合,赋予HA-Tyr水凝胶粘附信号并增强其生物活性。在RGD修饰的水凝胶上或之内培养的人脐静脉内皮细胞(HUVEC)显示出显着不同的粘附行为,从HA-Tyr水凝胶上的非粘附到苯酚2-聚(乙二醇)-RGD修饰的水凝胶上的强粘附。这种改变的细胞粘附行为导致了体外水凝胶中细胞增殖,迁移和毛细管状网络形成的改善。更重要的是,当HUVEC和人类成纤维细胞(HFF1)一起封装在RGD修饰的HA-Tyr水凝胶中时,皮下组织2周后,在充满细胞的凝胶内部观察到了功能性脉管系统。总之,将苯酚2-聚(乙二醇)-RGD原位偶联到HA-Tyr水凝胶系统中,再加上易于掺入细胞,提供了一种简单有效的方法来引入生物学信号,以制备多功能可注射水凝胶用于组织工程应用。

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