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Living biointerfaces based on non-pathogenic bacteria to direct cell differentiation

机译:基于非病原细菌的活生物界面指导细胞分化

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Genetically modified Lactococcus lactis , non-pathogenic bacteria expressing the FNIII7-10 fibronectin fragment as a protein membrane have been used to create a living biointerface between synthetic materials and mammalian cells. This FNIII7-10 fragment comprises the RGD and PHSRN sequences of fibronectin to bind α5β1 integrins and triggers signalling for cell adhesion, spreading and differentiation. We used L. lactis strain to colonize material surfaces and produce stable biofilms presenting the FNIII7-10 fragment readily available to cells. Biofilm density is easily tunable and remains stable for several days. Murine C2C12 myoblasts seeded over mature biofilms undergo bipolar alignment and form differentiated myotubes, a process triggered by the FNIII7-10 fragment. This biointerface based on living bacteria can be further modified to express any desired biochemical signal, establishing a new paradigm in biomaterial surface functionalisation for biomedical applications.
机译:基因改造的乳酸乳球菌(非乳杆菌)将FNIII 7-10 纤连蛋白片段表达为蛋白膜,已被用于在合成材料和哺乳动物细胞之间建立活的生物界面。 FNIII 7-10 片段包含纤连蛋白的RGD和PHSRN序列,可结合α5β1整联蛋白并触发细胞粘附,扩散和分化的信号传导。我们使用乳酸乳球菌菌株定殖在材料表面,并产生稳定的生物膜,呈现出可供细胞容易获得的FNIII 7-10 片段。生物膜密度很容易调节,并可以保持稳定数天。植入成熟生物膜上的鼠C2C12成肌细胞经历双极排列并形成分化的肌管,这一过程由FNIII 7-10 片段触发。这种基于活细菌的生物界面可以进一步修饰以表达任何所需的生化信号,从而为生物医学应用在生物材料表面功能化方面建立了新的范例。

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