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掺入ephrin-A1用于治疗性血管生成的合成仿生水凝胶。

Synthetic biomimetic hydrogels incorporated with ephrin-A1 for therapeutic angiogenesis.

作者信息

Moon James J, Lee Soo-Hong, West Jennifer L

机构信息

Department of Bioengineering, Rice University, P.O. Box 1892, MS 142, Houston, Texas 77251-1892, USA.

出版信息

Biomacromolecules. 2007 Jan;8(1):42-9. doi: 10.1021/bm060452p.

Abstract

Eph receptors and ephrin ligands are essential for vascular development and angiogenic remodeling. In this work, we developed biomimetic poly(ethylene glycol)-diacrylate hydrogels incorporated with ephrin-A1 and examined their angiogenic properties. Ephrin-A1 was covalently immobilized on the surface of hydrogels by chemical modification and photopolymerization. Ephrin-A1 immobilized on hydrogels was found to retain its capacity to stimulate endothelial cell adhesion in a dose-dependent manner as similar findings were observed on polystyrene culture wells pre-adsorbed with ephrin-A1. Cell adhesion stimulated by ephrin-A1 was abolished by treatment with soluble RGDS and anti-alpha(v)beta3 integrin but not anti-alpha(v)beta5 integrin antibodies, suggesting that ephrin-A1 activates cell adhesion through alpha(v)beta3 integrins. Also, surface immobilized ephrin-A1 was found to induce endothelial tubule formation with luminal diameters ranging 5-30 microm on hydrogels. The results of these studies demonstrate that pro-angiogenic properties of ephrin-A1 are preserved in hydrogels and suggest potential applications of this hydrogel system in regenerative medicine and tissue engineering.

摘要

Eph受体和ephrin配体对血管发育和血管生成重塑至关重要。在这项工作中,我们开发了掺入ephrin-A1的仿生聚乙二醇-二丙烯酸酯水凝胶,并研究了它们的血管生成特性。通过化学修饰和光聚合将ephrin-A1共价固定在水凝胶表面。发现固定在水凝胶上的ephrin-A1能够以剂量依赖性方式刺激内皮细胞粘附,这与在预先吸附有ephrin-A1的聚苯乙烯培养孔中观察到的结果相似。用可溶性RGDS和抗α(v)β3整合素抗体处理可消除ephrin-A1刺激的细胞粘附,但抗α(v)β5整合素抗体则不能,这表明ephrin-A1通过α(v)β3整合素激活细胞粘附。此外,发现表面固定的ephrin-A1可诱导水凝胶上形成管腔直径为5-30微米的内皮微管。这些研究结果表明,ephrin-A1的促血管生成特性在水凝胶中得以保留,并提示该水凝胶系统在再生医学和组织工程中的潜在应用。

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