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用于增强矿化和细胞黏附的纳米结构界面自组装肽-聚合物膜

Nanostructured interfacial self-assembled peptide-polymer membranes for enhanced mineralization and cell adhesion.

机构信息

3B's Research Group - Biomaterials, Biodegradables and Biomimetics, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, University of Minho, AvePark, 4806-909 Taipas, Guimarães, Portugal.

出版信息

Nanoscale. 2017 Sep 21;9(36):13670-13682. doi: 10.1039/c7nr03410e.

Abstract

Soft interfacial materials, such as self-assembled polymer membranes, are gaining increasing interest as biomaterials since they can provide selective barriers and/or controlled affinity interactions important to regulate cellular processes. Herein, we report the design and fabrication of multiscale structured membranes integrating selective molecular functionalities for potential applications in bone regeneration. The membranes were obtained by interfacial self-assembly of miscible aqueous solutions of hyaluronan and multi-domain peptides (MDPs) incorporating distinct biochemical motifs, including mineralizing (EE), integrin-binding (RGDS) and osteogenic (YGFGG) peptide sequences. Circular dichroism and Fourier transform infrared spectroscopy analyses of the MDPs revealed a predominant β-sheet conformation, while transmission electron microscopy (TEM) showed the formation of fibre-like nanostructures with different lengths. Scanning electron microscopy (SEM) of the membranes showed an anisotropic structure and surfaces with different nanotopographies, reflecting the morphological differences observed under TEM. All the membranes were able to promote the deposition of a calcium-phosphate mineral on their surface when incubated in a mineralizing solution. The ability of the MDPs, coated on coverslips or presented within the membranes, to support cell adhesion was investigated using primary adult periosteum-derived cells (PDCs) under serum-free conditions. Cells on the membranes lacking RGDS remained round, while in the presence of RGDS they appear to be more elongated and anchored to the membrane. These observations were confirmed by SEM analysis that showed cells attached to the membrane and exhibiting an extended morphology with close interactions with the membrane surface. We anticipate that these molecularly designed interfacial membranes can both provide relevant biochemical signals and structural biomimetic components for stem cell growth and differentiation and ultimately promote bone regeneration.

摘要

软质界面材料(如自组装聚合物膜)作为生物材料越来越受到关注,因为它们可以提供选择性的屏障和/或控制亲和相互作用,这对于调节细胞过程非常重要。在此,我们报告了具有多尺度结构的整合了选择性分子功能的界面膜的设计和制造,这些膜可能在骨再生中有应用。这些膜是通过透明质酸和多结构域肽(MDPs)的混合水溶液在界面处自组装得到的,其中包含不同的生化基序,包括矿化(EE)、整合素结合(RGDS)和成骨(YGFGG)肽序列。MDPs 的圆二色性和傅里叶变换红外光谱分析显示其主要为β-折叠构象,而透射电子显微镜(TEM)显示其形成了具有不同长度的纤维状纳米结构。膜的扫描电子显微镜(SEM)显示了各向异性结构和具有不同纳米形貌的表面,这反映了在 TEM 下观察到的形态差异。所有的膜在矿化溶液中孵育时都能够在其表面促进磷酸钙矿物的沉积。通过在无血清条件下使用原代成年骨膜衍生细胞(PDCs)研究涂覆在盖玻片上或存在于膜内的 MDPs 对细胞黏附的支持能力。缺乏 RGDS 的 MDP 涂层上的细胞仍保持圆形,而在存在 RGDS 的情况下,它们似乎更长且附着在膜上。SEM 分析证实了这一观察结果,表明细胞附着在膜上并呈现出与膜表面紧密相互作用的延伸形态。我们预计,这些分子设计的界面膜既能提供相关的生化信号,又能提供结构仿生成分,从而促进干细胞的生长和分化,并最终促进骨再生。

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