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将生物活性肽酶促偶联到可注射透明质酸-酪胺水凝胶系统中,以促进功能性脉管系统的形成。

Enzymatic conjugation of a bioactive peptide into an injectable hyaluronic acid-tyramine hydrogel system to promote the formation of functional vasculature.

机构信息

Institute of Bioengineering and Nanotechnology, 31 Biopolis Way, The Nanos, Singapore 138669, Singapore.

Institute of Bioengineering and Nanotechnology, 31 Biopolis Way, The Nanos, Singapore 138669, Singapore.

出版信息

Acta Biomater. 2014 Jun;10(6):2539-50. doi: 10.1016/j.actbio.2014.02.022. Epub 2014 Feb 21.

Abstract

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 2weeks 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.

摘要

在这项研究中,报告了一种一步酶介导制备多功能可注射透明质酸基水凝胶系统的方法。水凝胶是通过辣根过氧化物酶(HRP)和过氧化氢(H2O2)原位偶联酚基团形成的,并且在凝胶形成过程中同时将生物活性肽共轭到水凝胶中。通过合成含有酚基团的肽来制备这种多功能水凝胶,这些肽可以在 HRP 介导的交联反应中与透明质酸-酪胺(HA-Tyr)的酚基团偶联。初步研究表明,每个分子两个酚基团导致一致的高程度的共轭到 HA-Tyr 水凝胶网络中,与每个分子修饰一个酚基团不同。因此,设计了一个带有两个酚基团的精氨酸-甘氨酸-天冬氨酸(RGD)肽(phenol2-聚乙二醇-RGD)用于共轭,赋予 HA-Tyr 水凝胶粘附信号并增强其生物活性。在 RGD 修饰的水凝胶上或内部培养的人脐静脉内皮细胞(HUVECs)表现出明显不同的粘附行为,从在 HA-Tyr 水凝胶上不粘附到在修饰有 phenol2-聚乙二醇-RGD 的水凝胶上强烈粘附。这种改变的细胞粘附行为导致细胞在体外水凝胶中增殖、迁移和形成毛细血管样网络。更重要的是,当 HUVECs 和人成纤维细胞(HFF1)一起包封在 RGD 修饰的 HA-Tyr 水凝胶中时,在皮下组织中 2 周后,在细胞载凝胶内观察到功能性脉管系统。总之,将 phenol2-聚乙二醇-RGD 原位共轭到 HA-Tyr 水凝胶系统中,结合易于掺入细胞,为制备用于组织工程应用的多功能可注射水凝胶提供了一种简单有效的方法来引入生物信号。

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