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生物功能化的定向微凝胶为模仿复杂组织基质提供 3D 细胞导向。

Biofunctionalized aligned microgels provide 3D cell guidance to mimic complex tissue matrices.

机构信息

DWI - Leibniz-Institute for Interactive Materials, Aachen, Germany.

DWI - Leibniz-Institute for Interactive Materials, Aachen, Germany.

出版信息

Biomaterials. 2018 May;163:128-141. doi: 10.1016/j.biomaterials.2018.02.001. Epub 2018 Feb 9.

DOI:10.1016/j.biomaterials.2018.02.001
PMID:29459322
Abstract

Natural healing is based on highly orchestrated processes, in which the extracellular matrix plays a key role. To resemble the native cell environment, we introduce an artificial extracellular matrix (aECM) with the capability to template hierarchical and anisotropic structures in situ, allowing a minimally-invasive application via injection. Synthetic, magnetically responsive, rod-shaped microgels are locally aligned and fixed by a biocompatible surrounding hydrogel, creating a hybrid anisotropic hydrogel (Anisogel), of which the physical, mechanical, and chemical properties can be tailored. The microgels are rendered cell-adhesive with GRGDS and incorporated either inside a cell-adhesive fibrin or bioinert poly(ethylene glycol) hydrogel to strongly interact with fibroblasts. GRGDS-modified microgels inside a fibrin-based Anisogel enhance fibroblast alignment and lead to a reduction in fibronectin production, indicating successful replacement of structural proteins. In addition, YAP-translocation to the nucleus increases with the concentration of microgels, indicating cellular sensing of the overall anisotropic mechanical properties of the Anisogel. For bioinert surrounding PEG hydrogels, GRGDS-microgels are required to support cell proliferation and fibronectin production. In contrast to fibroblasts, primary nerve growth is not significantly affected by the biomodification of the microgels. In conclusion, this approach opens new opportunities towards advanced and complex aECMs for tissue regeneration.

摘要

自然愈合是基于高度协调的过程,其中细胞外基质起着关键作用。为了模拟天然细胞环境,我们引入了一种具有在原位模板化分级和各向异性结构能力的人工细胞外基质 (aECM),通过注射实现微创应用。合成的、对磁响应的棒状微凝胶通过生物相容性周围水凝胶局部对齐和固定,形成具有各向异性的混合水凝胶(Anisogel),其物理、机械和化学性质可以进行定制。微凝胶通过 GRGDS 变得具有细胞黏附性,并整合到细胞黏附性纤维蛋白或生物惰性聚乙二醇水凝胶中,与成纤维细胞强烈相互作用。纤维蛋白基 Anisogel 中的 GRGDS 修饰微凝胶增强了成纤维细胞的排列,并导致纤维连接蛋白产生减少,表明结构蛋白的成功替代。此外,随着微凝胶浓度的增加,YAP 向细胞核的易位增加,表明细胞对 Anisogel 的整体各向异性机械性能的感知。对于生物惰性的周围 PEG 水凝胶,GRGDS-微凝胶需要支持细胞增殖和纤维连接蛋白的产生。与成纤维细胞相比,神经的原发性生长不受微凝胶生物修饰的显著影响。总之,这种方法为组织再生提供了先进而复杂的 aECM 的新机会。

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