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Use of synthetic serum-free medium for culture of human dermal fibroblasts to establish an experimental system similar to living dermis

机译:使用合成的无血清培养基培养人真皮成纤维细胞以建立类似于活真皮的实验系统

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In this study, we sought to establish a defined experimental system for fibroblast growth similar to that of the living dermis. To this end, we evaluated the growth and biochemical characteristics of fibroblasts cultured with serum-free HFDM-1, a finely tuned synthetic medium for human fibroblast culture. Three culture conditions were used to grow fibroblasts obtained from primary culture: (1) culture with Dulbecco’s modified Eagle medium (DMEM) plus 10?% fetal bovine serum (serum-supplemented DMEM), (2) culture with DMEM (serum-free DMEM), and (3) culture with HFDM-1 (HFDM-1), and fibroblast morphology, growth, collagen type I production, and lipid composition were analyzed. Fibroblasts grown in HFDM-1 maintained cell numbers at nearly 100?% from days 14 to 21 and produced more collagen type I than cells grown in serum-supplemented and serum-free DMEM. Arachidonic acid (20:4) and total polyunsaturated fatty acids were lower in cells grown in serum-free DMEM and HFDM-1 than in serum-supplemented DMEM. These results suggested that HFDM-1 recapitulated growth conditions in the dermis better than traditional, serum-supplemented DMEM. In addition, the controlled chemical composition of HFDM-1 eliminated a potential source of variability in cell culture conditions.
机译:在这项研究中,我们试图为成纤维细胞的生长建立与活体真皮相似的确定的实验系统。为此,我们评估了用无血清HFDM-1(一种用于人体成纤维细胞培养的微调合成培养基)培养的成纤维细胞的生长和生化特性。三种培养条件用于培养从原代培养获得的成纤维细胞:(1)用Dulbecco改良的Eagle培养基(DMEM)加10%胎牛血清(补充血清的DMEM)培养,(2)用DMEM(无血清的DMEM)培养)和(3)用HFDM-1(HFDM-1)培养,分析成纤维细胞的形态,生长,I型胶原蛋白的产生和脂质组成。从第14天到第21天,在HFDM-1中生长的成纤维细胞保持的细胞数接近100%,并且比在补充血清和无血清的DMEM中生长的细胞产生更多的I型胶原。在无血清DMEM和HFDM-1中生长的细胞中花生四烯酸(20:4)和总多不饱和脂肪酸要低于在血清中补充DMEM的细胞。这些结果表明,HFDM-1重现了真皮中的生长条件,优于传统的补充血清的DMEM。此外,HFDM-1的化学成分受控,消除了细胞培养条件变异的潜在来源。

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