Protein fibrillar hydrogels for three-dimensional tissue engineering

Hui-cheng Yan, A. Nykänen, J. Ruokolainen, D. Farrar, A. Miller
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引用次数: 2

Abstract

Protein self-assembly into highly ordered fibrillar aggregates has attracted increasing attention over recent years, due primarily to its association with disease states such as Alzheimer's. More recently, however, research has focused on understanding the generic behavior of protein self-assembly where fibrillation is typically induced under harsh conditions of low pH and/or high temperature. Moreover the inherent properties of these fibrils, including their nanoscale dimension, environmental responsiveness, and biological compatibility, are attracting substantial interest for exploiting these fibrils for the creation of new materials. Here we will show how protein fibrils can be formed under physiological conditions and their subsequent gelation driven using the ionic strength of cell culture media while simultaneously incorporating cells homogeneously throughout the gel network. The fibrillar and elastic nature of the gel have been confirmed using cryo-transmission electron microscopy and oscillatory rheology, respectively; while cell culture work shows that our hydrogels promote cell spreading, attachment, and proliferation in three dimensions.
三维组织工程用蛋白纤维水凝胶
蛋白质自组装成高度有序的纤维聚集体近年来引起了越来越多的关注,主要是因为它与阿尔茨海默病等疾病状态有关。然而,最近的研究集中在了解蛋白质自组装的一般行为,其中纤颤通常在低pH和/或高温的恶劣条件下诱导。此外,这些原纤维的固有特性,包括它们的纳米级尺寸、环境响应性和生物相容性,正吸引着人们对利用这些原纤维制造新材料的极大兴趣。在这里,我们将展示如何在生理条件下形成蛋白原纤维,并利用细胞培养基的离子强度驱动其随后的凝胶化,同时在整个凝胶网络中均匀地结合细胞。凝胶的纤维性和弹性性质已分别用冷冻透射电镜和振荡流变学证实;而细胞培养工作表明,我们的水凝胶促进细胞在三维上的扩散、附着和增殖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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