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植入多孔生物材料中的不同血管生成模式和内皮反应。

Different angiogenesis modes and endothelial responses in implanted porous biomaterials.

作者信息

Zhan Kuihua, Bai Lun, Wang Guangqian, Zuo Baoqi, Xie Liang, Wang Xinhong

机构信息

School of Mechanical and Electric Engineering, Soochow University, 8 Jixue Road, Suzhou, 215131, China.

出版信息

Integr Biol (Camb). 2018 Jul 16;10(7):406-418. doi: 10.1039/c8ib00061a.

Abstract

An in vivo experimental model based on implanting porous biomaterials to study angiogenesis was proposed. In the implanted porous polyvinyl alcohol, three major modes of angiogenesis, sprouting, intussusception and splitting, were found. By electron microscopy and three-dimensional simulation of the angiogenic vessels, we investigated the morphological characteristics of the three modes and paid special attention to the initial morphological difference between intussusception and splitting, and it was confirmed that the endothelial abluminal invagination and intraluminal protrusion are pre-representations of intussusception and splitting, respectively. Based on immunohistochemical analysis of HIF-1α, VEGF and Flt-1 expressions, it was demonstrated that the dominant mode of angiogenesis is related to the local hypoxic condition, and that there is difference in the response of endothelial cells to hypoxia-induced VEGF between sprouting and splitting. Specifically, in the biomaterials implanted for 3 days, the higher expression and gradient of VEGF induced by severe hypoxia in the avascular area caused sprouting of the peripheral capillaries, and in the biomaterial implanted for 9 days, with moderate hypoxia, splitting became a dominant mode. Whether on day 3 or day 9, Flt-1 expression in sprouting endothelia was significantly higher than that in splitting endothelia, which indicates that sprouting is caused by the strong response of endothelial cells to VEGF, while splitting is associated with their weaker response. As a typical experimental example, these results show the effectiveness of the porous biomaterial implantation model for studying angiogenesis, which is expected to become a new general model.

摘要

提出了一种基于植入多孔生物材料来研究血管生成的体内实验模型。在植入的多孔聚乙烯醇中,发现了血管生成的三种主要模式,即芽生、套入和分裂。通过电子显微镜和血管生成血管的三维模拟,我们研究了这三种模式的形态特征,并特别关注套入和分裂之间的初始形态差异,证实内皮细胞腔外内陷和腔内突出分别是套入和分裂的预表现形式。基于对HIF-1α、VEGF和Flt-1表达的免疫组织化学分析,表明血管生成的主导模式与局部缺氧状况有关,并且芽生和分裂的内皮细胞对缺氧诱导的VEGF的反应存在差异。具体而言,在植入3天的生物材料中,无血管区域严重缺氧诱导的VEGF的较高表达和梯度导致外周毛细血管芽生,而在植入9天的生物材料中,中度缺氧时分裂成为主导模式。无论是在第3天还是第9天,芽生内皮细胞中的Flt-1表达均显著高于分裂内皮细胞中的表达,这表明芽生是由内皮细胞对VEGF的强烈反应引起的,而分裂则与其较弱的反应有关。作为一个典型的实验例子,这些结果表明了多孔生物材料植入模型在研究血管生成方面的有效性,有望成为一种新的通用模型。

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