Eanes R Z
In Vitro Cell Dev Biol. 1985 Jun;21(6):328-32. doi: 10.1007/BF02691580.
A fluorometric procedure for measuring DNA was used to study growth and metabolic responses of eight cell strains of human foreskin fibroblasts. In preliminary studies this procedure gave more precise specific activity changes in N-acetyl-beta-D-glucosaminidase (NAG) than did a protein activity basis, when changes in this enzyme's specific activity were investigated as a function of experimental cell manipulation. When fibroblast growth in eight cell strains was compared in 134 mM D-fructose vs. 13.4 mM glucose-supplemented minimum essential media, a significant increase in cellular DNA (50%) and protein (45%) occurred over an 11-d period. No significant differences in media pH change, lactate production, or carbohydrate uptake occurred on a DNA basis when cell metabolism was compared over the last 24 h of culture in the two media. Cells grown in fructose-containing media tended to show a reduction in NAG specific activity when compared with those grown in glucose-containing media.
采用一种测量DNA的荧光测定法,研究了8种人包皮成纤维细胞系的生长和代谢反应。在初步研究中,当研究该酶比活性变化作为实验性细胞操作的函数时,与基于蛋白质活性的方法相比,该方法在N-乙酰-β-D-氨基葡萄糖苷酶(NAG)中给出了更精确的比活性变化。当在补充有134 mM D-果糖与13.4 mM葡萄糖的最低必需培养基中比较8种细胞系中的成纤维细胞生长时,在11天的时间内细胞DNA(50%)和蛋白质(45%)显著增加。当在两种培养基中培养的最后24小时比较细胞代谢时,基于DNA的培养基pH变化、乳酸产生或碳水化合物摄取没有显著差异。与在含葡萄糖培养基中生长的细胞相比,在含果糖培养基中生长的细胞倾向于显示NAG比活性降低。