Iglewski W J, Taylor A, Hodges R, Tolle J
Infect Immun. 1979 Nov;26(2):458-61. doi: 10.1128/iai.26.2.458-461.1979.
Different methods were used to assay diphtheria toxin sensitivity of fibroblast and heart cell cultures from chicken embryos of various ages. As defined by inhibition of protein synthesis, fibroblasts from 18-day and younger embryos respond more rapidly to toxin than fibroblasts from older embryos. The response of heart cells cultures is independent of the age of the embryos and is similar to the response of fibroblasts from 18-day embryos. Since the EF-2 content is 10-fold less in fibroblasts from 21-day-old embryos, the different responses of protein synthesis to intoxication appear to reside at the membrane level. Cytotoxicity assays in cell culture and in vivo toxin sensitivity assays show that cells from both young and old embryos, as well as whole embryos, are equally sensitive to toxin. Thus, short-term (5-h) measurements of inhibition of protein synthesis are insufficient for determining the relative sensitivity of cells to intoxication as defined by cell death.
采用不同方法检测了不同日龄鸡胚成纤维细胞和心脏细胞培养物对白喉毒素的敏感性。根据蛋白质合成抑制情况来定义,18日龄及更小日龄胚胎的成纤维细胞比大龄胚胎的成纤维细胞对毒素的反应更快。心脏细胞培养物的反应与胚胎日龄无关,与18日龄胚胎的成纤维细胞反应相似。由于21日龄胚胎的成纤维细胞中延伸因子2(EF-2)含量少10倍,蛋白质合成对中毒的不同反应似乎存在于膜水平。细胞培养中的细胞毒性检测和体内毒素敏感性检测表明,幼龄和老龄胚胎的细胞以及整个胚胎对毒素的敏感性相同。因此,对于确定细胞对由细胞死亡定义的中毒的相对敏感性而言,短期(5小时)蛋白质合成抑制测量是不够的。