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具有定制黏附性和可降解性的合成细胞外基质在血管生成发芽过程中支持管腔形成。

Synthetic extracellular matrices with tailored adhesiveness and degradability support lumen formation during angiogenic sprouting.

机构信息

Bioactive Materials Laboratory, Max Planck Institute for Molecular Biomedicine, Münster, Germany.

Electron Microscopy Unit, Max Planck Institute for Molecular Biomedicine, Münster, Germany.

出版信息

Nat Commun. 2021 Jun 7;12(1):3402. doi: 10.1038/s41467-021-23644-5.

Abstract

A major deficit in tissue engineering strategies is the lack of materials that promote angiogenesis, wherein endothelial cells from the host vasculature invade the implanted matrix to form new blood vessels. To determine the material properties that regulate angiogenesis, we have developed a microfluidic in vitro model in which chemokine-guided endothelial cell sprouting into a tunable hydrogel is followed by the formation of perfusable lumens. We show that long, perfusable tubes only develop if hydrogel adhesiveness and degradability are fine-tuned to support the initial collective invasion of endothelial cells and, at the same time, allow for matrix remodeling to permit the opening of lumens. These studies provide a better understanding of how cell-matrix interactions regulate angiogenesis and, therefore, constitute an important step towards optimal design criteria for tissue-engineered materials that require vascularization.

摘要

组织工程策略的一个主要缺陷是缺乏促进血管生成的材料,其中宿主脉管系统中的内皮细胞侵入植入的基质以形成新的血管。为了确定调节血管生成的材料特性,我们开发了一种微流控体外模型,其中趋化因子引导内皮细胞向可调节水凝胶中发芽,然后形成可灌注的管腔。我们表明,如果精细调节水凝胶的粘附性和可降解性以支持内皮细胞的初始集体入侵,同时允许基质重塑以允许管腔开放,则只有长的、可灌注的管才能形成。这些研究更好地了解了细胞-基质相互作用如何调节血管生成,因此,为需要血管化的组织工程材料的最佳设计标准构成了重要的一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1c4/8184799/29504c591f77/41467_2021_23644_Fig1_HTML.jpg

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