天然和合成生物材料血管生成的直接比较:基质孔隙度调节内皮细胞侵袭速度和萌芽直径

William Y. Wang, Robert N. Kent III, Stephanie A. Huang, Evan H. Jarman, Eve H. Shikanov, Christopher D. Davidson, Harrison L. Hiraki, Daphne Lin, M. A. Wall, Jae-Won Shin, W. Polacheck, A. Shikanov, Brendon M. Baker
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引用次数: 0

摘要

大型、扩散受阻的生物材料植入物的血管化需要了解细胞外基质(ECM)的特性如何调节血管生成。在许多不同的血管生成分析中评估的各种生物材料都强调了影响这一复杂多细胞过程的ECM决定因素。然而,丰富的材料平台,每个都有独特的参数来模拟内皮细胞(EC)发芽,这给研究之间的解释和比较带来了额外的挑战。在这项工作中,我们直接比较了常用的天然(胶原蛋白和纤维蛋白)和合成葡聚糖乙烯基砜(DexVS)水凝胶在多路血管生成芯片平台上的血管生成潜力。调节胶原蛋白和纤维蛋白水凝胶的基质密度证实了先前的发现,即基质密度的增加对应于连接的多细胞芽中EC入侵的增加,但入侵速度减慢。然而,合成DexVS水凝胶中的血管生成导致较少的多细胞芽。通过表征水凝胶杨氏模量和渗透率(一种测量基质孔隙度的方法),我们发现基质渗透率与EC侵入深度和发芽直径显著相关。虽然微孔胶原蛋白和纤维蛋白水凝胶在体外产生了流光化芽,但它们在植入后迅速被吸收到小鼠附睾脂肪垫中。相比之下,DexVS水凝胶被证明相对稳定。为了增强DexVS水凝胶中的血管生成,我们加入了牺牲微凝胶,在整个水凝胶中产生细胞尺度的孔隙。微孔DexVS水凝胶在体外使芽胞流光化,并增强了细胞在体内的侵袭。为了设计用于长期再生治疗的血管化生物材料,这项工作表明,合成生物材料在植入后提供了更好的尺寸和形状控制,并且调节基质孔隙率可以更好地支持宿主血管生成。
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Direct Comparison of Angiogenesis in Natural and Synthetic Biomaterials Reveals Matrix Porosity Regulates Endothelial Cell Invasion Speed and Sprout Diameter
Vascularization of large, diffusion-hindered biomaterial implants requires an understanding of how extracellular matrix (ECM) properties regulate angiogenesis. Sundry biomaterials assessed across many disparate angiogenesis assays have highlighted ECM determinants that influence this complex multicellular process.  However, the abundance of material platforms, each with unique parameters to model endothelial cell (EC) sprouting presents additional challenges of interpretation and comparison between studies. In this work we directly compared the angiogenic potential of commonly utilized natural (collagen and fibrin) and synthetic dextran vinyl sulfone (DexVS) hydrogels in a multiplexed angiogenesis-on-a-chip platform. Modulating matrix density of collagen and fibrin hydrogels confirmed prior findings that increases in matrix density correspond to increased EC invasion as connected, multicellular sprouts, but with decreased invasion speeds. Angiogenesis in synthetic DexVS hydrogels, however, resulted in fewer multicellular sprouts. Characterizing hydrogel Young’s modulus and permeability (a measure of matrix porosity), we identified matrix permeability to significantly correlate with EC invasion depth and sprout diameter. Although microporous collagen and fibrin hydrogels produced lumenized sprouts in vitro, they rapidly resorbed post-implantation into the murine epididymal fat pad. In contrast, DexVS hydrogels proved comparatively stable. To enhance angiogenesis within DexVS hydrogels, we incorporated sacrificial microgels to generate cell-scale pores throughout the hydrogel. Microporous DexVS hydrogels resulted in lumenized sprouts in vitro and enhanced cell invasion in vivo . Towards the design of vascularized biomaterials for long-term regenerative therapies, this work suggests that synthetic biomaterials offer improved size and shape control following implantation and that tuning matrix porosity may better support host angiogenesis.
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