Biomedical Optics and Applied Biophysics Laboratory, Division of Electromagnetics, Electrooptics and Electronic Materials, School of Electrical and Computer Engineering, National Technical University of Athens, 9 Iroon Polytechniou, Athens 15780 Greece.
Biomedical Optics and Applied Biophysics Laboratory, Division of Electromagnetics, Electrooptics and Electronic Materials, School of Electrical and Computer Engineering, National Technical University of Athens, 9 Iroon Polytechniou, Athens 15780 Greece.
Mater Sci Eng C Mater Biol Appl. 2014 Dec;45:455-68. doi: 10.1016/j.msec.2014.09.006. Epub 2014 Sep 28.
Collagen is the major fibrous extracellular matrix protein and due to its unique properties, it has been widely used as biomaterial, scaffold and cell-substrate. The aim of the paper was to use Atomic Force Microscopy (AFM) in order to investigate well-characterized collagen thin films after ultraviolet light (UV) irradiation. The films were also used as in vitro culturing substrates in order to investigate the UV-induced alterations to fibroblasts. A special attention was given in the alteration on collagen D-periodicity. For short irradiation times, spectroscopy (fluorescence/absorption) studies demonstrated that photodegradation took place and AFM imaging showed alterations in surface roughness. Also, it was highlighted that UV-irradiation had different effects when it was applied on collagen solution than on films. Concerning fibroblast culturing, it was shown that fibroblast behavior was affected after UV irradiation of both collagen solution and films. Furthermore, after a long irradiation time, collagen fibrils were deformed revealing that collagen fibrils are consisting of multiple shells and D-periodicity occurred on both outer and inner shells. The clarification of the effects of UV light on collagen and the induced modifications of cell behavior on UV-irradiated collagen-based surfaces will contribute to the better understanding of cell-matrix interactions in the nanoscale and will assist in the appropriate use of UV light for sterilizing and photo-cross-linking applications.
胶原蛋白是主要的纤维细胞外基质蛋白,由于其独特的性质,已被广泛用作生物材料、支架和细胞基质。本文的目的是使用原子力显微镜(AFM)研究经紫外线(UV)照射后的特性明确的胶原蛋白薄膜。这些薄膜还被用作体外培养底物,以研究 UV 诱导对成纤维细胞的改变。特别关注胶原蛋白 D-周期性的改变。对于短的辐照时间,光谱(荧光/吸收)研究表明发生了光降解,AFM 成像显示表面粗糙度发生了改变。此外,还强调了 UV 照射对溶液中的胶原蛋白和薄膜中的胶原蛋白有不同的影响。关于成纤维细胞培养,研究表明,UV 照射胶原蛋白溶液和薄膜后,成纤维细胞的行为受到影响。此外,经过长时间的辐照后,胶原纤维发生变形,表明胶原纤维由多个壳层组成,D-周期性发生在外层和内层。阐明了 UV 光对胶原蛋白的影响以及 UV 辐照胶原基表面对细胞行为的诱导修饰,将有助于更好地理解纳米尺度上细胞与基质的相互作用,并有助于适当使用 UV 光进行杀菌和光交联应用。