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血管内皮生长因子、成纤维细胞生长因子-2和血小板衍生生长因子的阶段性亲和控制递送可增强体外血管生成。

Phased affinity-controlled delivery of vascular endothelial growth factor, fibroblast growth factor-2, and platelet derived growth factor enhances in vitro angiogenesis.

作者信息

Svendsen Justin E, Asnes Chandler L, Nightheart Samuel R, Ford Madeleine R, Hajarizadeh Armaan, Oh Simon C, Hochstatter Henry B, O'Hara-Smith Johnathan R, Guldberg Robert E, Hettiaratchi Marian H

出版信息

bioRxiv. 2025 Jul 4:2025.07.01.662647. doi: 10.1101/2025.07.01.662647.

Abstract

Angiogenesis, the growth of vasculature from existing blood vessels, requires the coordinated secretion of multiple angiogenic growth factors that each stimulate the cellular recruitment, patterning, and morphogenesis inherent to vascular network formation. Among these secreted factors, vascular endothelial growth factor (VEGF), fibroblast growth factor-2 (FGF-2), and platelet derived growth factor (PDGF) amplify key stages of angiogenesis. Disruptions in their secretion have been implicated in poor vascular network formation. Current methods for exploring variations in the phased presentation of multiple different proteins are limited, which has restricted our ability to explore the effect of growth factor timing on angiogenesis. To address this knowledge gap, we developed affibodies, which are alpha-helical binding proteins, to phase the release of VEGF-165, FGF-2, and PDGF-BB from a single drug delivery vehicle via specific protein-affibody affinity interactions. We used yeast surface display to engineer three VEGF-, three FGF-2-, and two PDGF-specific affibodies with different affinities for their target proteins. We demonstrated that the cumulative release of VEGF and FGF-2 are inversely correlated with the strength of the protein-affibody affinity interaction and that hydrogels containing multiple protein-specific affibodies can independently control the release of VEGF, FGF-2, and PDGF, largely in accordance with the strength of the affinity interactions. Using a rat-derived intact microvascular fragment model of in vitro angiogenesis, we revealed that sequential delivery of soluble VEGF, followed by FGF-2, and then PDGF enhances vascular network formation and branching. We then designed an affibody-conjugated hydrogel to mimic this sequence of protein delivery, resulting in increased vascular branching and network length compared to all other hydrogel compositions and the sequential delivery of soluble growth factors. This work establishes a new platform for modulating the timing of growth factor delivery, enabling the exploration of how temporal variations in protein secretion impact regeneration and development.

摘要

血管生成,即从现有血管生长出新的脉管系统,需要多种血管生成生长因子的协同分泌,每种因子都能刺激细胞募集、模式形成以及血管网络形成所固有的形态发生。在这些分泌因子中,血管内皮生长因子(VEGF)、成纤维细胞生长因子 -2(FGF-2)和血小板衍生生长因子(PDGF)会放大血管生成的关键阶段。它们分泌的紊乱与不良的血管网络形成有关。目前探索多种不同蛋白质阶段性呈现变化的方法有限,这限制了我们探究生长因子释放时间对血管生成影响的能力。为了填补这一知识空白,我们开发了亲和体,即α - 螺旋结合蛋白,通过特定的蛋白质 - 亲和体亲和相互作用,使VEGF - 165、FGF - 2和PDGF - BB从单一药物递送载体中按阶段释放。我们利用酵母表面展示技术设计了三种对VEGF、三种对FGF - 2以及两种对PDGF具有不同亲和力的特异性亲和体。我们证明VEGF和FGF - 2的累积释放与蛋白质 - 亲和体亲和相互作用的强度呈负相关,并且含有多种蛋白质特异性亲和体的水凝胶能够独立控制VEGF、FGF - 2和PDGF的释放,这在很大程度上与亲和相互作用的强度一致。使用大鼠来源的体外血管生成完整微血管片段模型,我们发现先依次递送可溶性VEGF,接着是FGF - 2,然后是PDGF,可增强血管网络形成和分支。然后我们设计了一种亲和体偶联水凝胶来模拟这种蛋白质递送序列,与所有其他水凝胶组合物以及可溶性生长因子的顺序递送相比,其血管分支和网络长度增加。这项工作建立了一个用于调节生长因子递送时间的新平台,能够探究蛋白质分泌的时间变化如何影响再生和发育。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66bb/12236655/067c1a416679/nihpp-2025.07.01.662647v1-f0002.jpg

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