Silva Joana M, García José R, Reis Rui L, García Andrés J, Mano João F
3B's Research Group - Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence of Tissue Engineering and Regenerative Medicine, Avepark - Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Barco GMR, Portugal; ICVS/3B's - PT Government Associate Laboratory, 4710-243 Braga/Guimarães, Portugal.
Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA 30332, USA; Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA.
Acta Biomater. 2017 Mar 15;51:279-293. doi: 10.1016/j.actbio.2017.01.058. Epub 2017 Jan 23.
Understanding the mechanisms controlling cell-multilayer film interactions is crucial to the successful engineering of these coatings for biotechnological and biomedical applications. Herein, we present a strategy to tune the cell adhesive properties of multilayers based on marine polysaccharides with and without cross-linking and/or coating with extracellular matrix proteins. Chemical cross-linking of multilayers improved mechanical properties of the coatings but also elicited changes in surface chemistry that alter the adhesion of human umbilical vein endothelial cells. We evaluated a strategy to decouple the mechanical and chemical properties of these films, enabling the transition from cell-adhesive to cell-resistant multilayers. Addition of chitosan/alginate multilayers on top of cross-linked films decreased endothelial cell adhesion, spreading, and proliferation to similar levels as uncross-linked films. Our findings highlight the key role of surface chemistry in cell-multilayer film interactions, and these engineered nanocoatings represent a tunable model of cell adhesive and non-adhesive multilayered films.
Multilayered films based on marine-derived polysaccharides were obtained by layer-by-layer (LbL). Biological tests with human umbilical vein endothelial cells (HUVECs) showed the potential of these films to tailor cell adhesion, spreading and proliferation. These multilayered films promise to be versatile and tunable model of cell adhesive and non-adhesive films.
了解控制细胞与多层膜相互作用的机制对于成功设计用于生物技术和生物医学应用的这些涂层至关重要。在此,我们提出了一种基于海洋多糖的多层膜细胞粘附特性调控策略,该多层膜有或没有交联和/或用细胞外基质蛋白包被。多层膜的化学交联改善了涂层的机械性能,但也引发了表面化学变化,从而改变了人脐静脉内皮细胞的粘附。我们评估了一种使这些膜的机械和化学性质解耦的策略,实现了从细胞粘附性多层膜到细胞抗性多层膜的转变。在交联膜上添加壳聚糖/海藻酸盐多层膜可使内皮细胞的粘附、铺展和增殖降低至与未交联膜相似的水平。我们的研究结果突出了表面化学在细胞与多层膜相互作用中的关键作用,并且这些工程化纳米涂层代表了一种可调节的细胞粘附和非粘附多层膜模型。
基于海洋来源多糖的多层膜通过层层组装(LbL)获得。用人脐静脉内皮细胞(HUVECs)进行的生物学测试表明这些膜具有调节细胞粘附、铺展和增殖的潜力。这些多层膜有望成为细胞粘附和非粘附膜的通用且可调节模型。