Preparation of recombinant human-like collagen/fibroin scaffold and its promoting effect on vascular cells biocompatibility. (July 2018)

• Record Type: Journal Article
• Authors: Yan, Jia; Hu, Kun; Xiao, YongHao; Zhang, Fan; Han, Lu; Pan, Shun; Li, LuHai; Wei, Yen; Cui, FuZhai
• Is Part Of: Journal of bioactive and compatible polymers. Volume 33:Number 4(2018:Jul.)
• Page Start: 416
• Page End: 425
• Publication Date: 2018-07
• Subjects: recombinant human-like collagen -- fibroin -- scaffold -- vascular smooth muscle cells -- biomaterial; Biomedical materials -- Periodicals; Polymers in medicine -- Periodicals; Polymers -- Periodicals; 547.7
• DOI: 10.1177/0883911518769680
• Languages: English
• ISSNs: 0883-9115

Abstract

A novel recombinant human-like collagen/fibroin scaffold has been prepared previously, which has high porosity, controllable pore size, and much better mechanical properties than the reported fibroin-based scaffold. In this research, the cell responses of vascular smooth muscle cells to this blend scaffold were examined in vitro. Cell morphology, adherence, and growth in scaffolds were observed by scanning electron microscopy, laser scanning confocal microscopy after staining of the cells with propidium iodide at 1, 3, 5, and 7 days, respectively. A wide range of measurements, including 3-[4, 5–dimethylthiazol-2-yl]-2, 5-diphenyl tetrasodium bromide assay, and total intracellular protein content at the end of 7 days culture, were conducted. An increase of viability and protein content of vascular smooth muscle cells cultured in recombinant human-like collagen/fibroin scaffold was found. The laser scanning confocal microscopy and scanning electron microscopy results confirm that the cells readily adhered and proliferation in the blend than in fibroin scaffold, and indicate a better adhesion process. The positive effects were especially significant for vascular smooth muscle cells. The recombinant human-like collagen/fibroin scaffold could be a promising biomaterial for vascular tissue engineering.