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硫酸化和磷酸化琼脂糖作为用于FGF-2释放的仿生模式的生物材料。

Sulfated and Phosphorylated Agarose as Biomaterials for a Biomimetic Paradigm for FGF-2 Release.

作者信息

Forget Aurelien, Shastri V Prasad

机构信息

Institute for Macromolecular Chemistry, Stefan-Meier-Strasse 31, 79104 Freiburg, Germany.

BIOSS, Centre for Biological Signalling, Schanzelstrasse 18, 79104 Freiburg, Germany.

出版信息

Biomimetics (Basel). 2024 Dec 30;10(1):12. doi: 10.3390/biomimetics10010012.

Abstract

Cardiovascular diseases such as myocardial infarction or limb ischemia are characterized by regression of blood vessels. Local delivery of growth factors (GFs) involved in angiogenesis such as fibroblast blast growth factor-2 (FGF-2) has been shown to trigger collateral neovasculature and might lead to a therapeutic strategy. In vivo, heparin, a sulfated polysaccharide present in abundance in the extracellular matrix (ECM), has been shown to function as a local reservoir for FGF-2 by binding FGF-2 and other morphogens and it plays a role in the evolution of GF gradients. To access injectable biomaterials that can mimic such natural electrostatic interactions between soluble signals and macromolecules and mechanically tunable environments, the backbone of agarose, a thermogelling marine-algae-derived polysaccharide, was modified with sulfate, phosphate, and carboxylic moieties and the interaction and release of FGF-2 from these functionalized hydrogels was assessed by ELISA in vitro and CAM assay in ovo. Our findings show that FGF-2 remains active after release, and FGF-2 release profiles can be influenced by sulfated and phosphorylated agarose, and in turn, promote varied blood vessel formation kinetics. These modified agaroses offer a simple approach to mimicking electrostatic interactions experienced by GFs in the extracellular environment and provide a platform to probe the role of these interactions in the modulation of growth factor activity and may find utility as an injectable gel for promoting angiogenesis and as bioinks in 3D bioprinting.

摘要

诸如心肌梗死或肢体缺血等心血管疾病的特征是血管退化。已表明,局部递送参与血管生成的生长因子(GFs),如成纤维细胞生长因子-2(FGF-2),可触发侧支新生血管形成,并可能带来一种治疗策略。在体内,肝素是细胞外基质(ECM)中大量存在的一种硫酸化多糖,已表明它可通过结合FGF-2和其他形态发生素来充当FGF-2的局部储存库,并在生长因子梯度的形成中发挥作用。为了获得能够模拟可溶性信号与大分子之间这种自然静电相互作用以及机械可调环境的可注射生物材料,对琼脂糖(一种热凝胶化的海洋藻类衍生多糖)的主链进行了硫酸化、磷酸化和羧基修饰,并通过体外ELISA和鸡胚绒毛尿囊膜(CAM)试验评估了FGF-2从这些功能化水凝胶中的相互作用和释放情况。我们的研究结果表明,FGF-2释放后仍保持活性,FGF-2的释放曲线可受硫酸化和磷酸化琼脂糖的影响,进而促进不同的血管形成动力学。这些修饰后的琼脂糖提供了一种简单方法来模拟生长因子在细胞外环境中经历的静电相互作用,并提供了一个平台来探究这些相互作用在调节生长因子活性中的作用,并且可能作为促进血管生成的可注射凝胶以及3D生物打印中的生物墨水发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2074/11761575/48efb30c32ef/biomimetics-10-00012-g0A1.jpg

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