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Enhancing vascularization of a gelatin-based micro-cavitary hydrogel by increasing the density of the micro-cavities

机译:通过增加微腔的密度来增强基于明胶的微腔水凝胶的血管形成

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摘要

The transport of nutrients and oxygen by vascular networks into engineered tissue constructs is critical to their successful integration into host tissues. Hydrogel has achieved some promising results as scaffolds for vascularization. However, the vascularization of hydrogel is still constrained by its inherent submicron- or nano-sized pores. In this study, two gelatin-based micro-cavitary gel (Gel-MCG) constructs with varying densities of micro-cavities were developed with a photocrosslinkable gelatin methacrylate (Gel-MA) precursor and porogenic gelatin microspheres (MS), and their functions in supporting vascularization within hydrogels were evaluated with endothelial progenitor outgrowth cells (EPOCs). The increase of cavitary density could enhance the vascularization of Gel-MCG constructs. After 14 d of culture in vitro, the vascularization of Gel-MCG constructs with higher cavitary density was significantly superior to that of gelatin spongy control and the fusion of vascularized cavities in the constructs could be observed. Further subcutaneous implantation of the Gel-MCG constructs with higher cavitary density into nude mice also showed obvious vascular invasion from host tissues. Taken together, these results indicate that the increase in cavitary density can efficiently facilitate the vascularization of Gel-MCG constructs both in vitro and in vivo and that such highly-porous Gel-MCG constructs have great potential to be a promising scaffold for the development of vascularized tissue constructs.
机译:通过血管网络将营养物和氧气输送到工程组织构造中,对于它们成功整合到宿主组织中至关重要。水凝胶作为血管生成支架取得了一些有希望的结果。然而,水凝胶的血管形成仍然受到其固有的亚微米或纳米级孔的限制。在这项研究中,开发了两种具有不同微腔密度的基于明胶的微腔凝胶(Gel-MCG)构建体,它们使用可光交联的甲基丙烯酸明胶(Gel-MA)前体和成孔明胶微球(MS)开发,并在用内皮祖细胞(EPOC)评估支持水凝胶内的血管形成。空化密度的增加可以增强Gel-MCG构建体的血管化。体外培养14 d后,具有较高空化密度的Gel-MCG构建体的血管形成明显优于明胶海绵对照,并且可以观察到血管化空腔在构建物中的融合。将具有较高空化密度的Gel-MCG构建体进一步皮下植入裸鼠也显示出明显的血管从宿主组织侵入。综上所述,这些结果表明,腔密度的增加可以有效地促进Gel-MCG构建体在体外和体内的血管化,并且这种高度多孔的Gel-MCG构建体具有巨大的潜力,有望成为发展Glu-MCG构建体的有希望的支架。血管化的组织结构。

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