Bogen Kenneth T, Arnold Lora L, Chowdhury Aparajita, Pennington Karen L, Cohen Samuel M
Health Sciences, Oakland, CA, USA.
Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, USA.
Toxicol Rep. 2016 Dec 14;4:32-38. doi: 10.1016/j.toxrep.2016.12.003. eCollection 2017.
The arsenite (As) cytotoxicity dose-response (DR) of human keratinocytes (HEK001) was examined at greater statistical resolution than ever previously reported using the MTT assay to determine cell viability. Fifty-four 96-well plates were treated with As concentrations of 0.25, 0.5, 1, 2, 3, 4, 5, 7, 10, 15, 20, 25, or 30 μM. Because of unexpected variation in viability response patterns, a two-stage DR analysis was used in which data on plate-specific viability (%), estimated as 100% times the ratio of measured viability in exposed to unexposed cells, were fit initially to a generalized lognormal response function positing that HEK001 cells studied consisted of: a proportion of relatively highly sensitive (HS) cells, a proportion of relatively resistant cells, and a remaining (1--) fraction of typical-sensitivity (TS) cells exhibiting the intermediate level of As sensitivity characteristic of most cells in each assay. The estimated fractions and were used to adjust data from all 54 plates (and from the 28 plates yielding the best fits) to reflect the condition that = = 0 to provide detailed DR analysis specifically for TS cells. Four DR models fit to the combined adjusted data were each very predictive (R > 0.97) overall but were inconsistent with at least one of the data set examined (p < 10). Adjusted mean responses at ≤3 μM were approximately equal (p > 0.30) and exceeded 100% significance (p ≤ 10). A low-dose hormetic model provided the best fit to the combined adjusted data for TS cells (R = 0.995). Marked variability in estimates of (the proportion of apparent HS cells) was unexpected, not readily explained, and warrants further study using additional cell lines and assay methods, and .
使用MTT法检测细胞活力,以比以往报道更高的统计分辨率,研究了亚砷酸盐(As)对人角质形成细胞(HEK001)的细胞毒性剂量反应(DR)。用浓度为0.25、0.5、1、2、3、4、5、7、10、15、20、25或30μM的As处理54个96孔板。由于活力反应模式存在意外变化,采用两阶段DR分析,其中将特定板活力(%)数据(估计为暴露细胞与未暴露细胞中测量活力之比的100倍)最初拟合到广义对数正态反应函数,该函数假定所研究的HEK001细胞由以下部分组成:一定比例的相对高敏感(HS)细胞、一定比例的相对抗性细胞,以及其余(1 - -)比例的表现出每次试验中大多数细胞典型敏感性(TS)中间水平的典型敏感性(TS)细胞。估计的比例和用于调整所有54个板(以及28个拟合最佳的板)的数据,以反映 = = 0的条件,从而专门针对TS细胞进行详细的DR分析。拟合合并调整后数据的四个DR模型总体上都具有很强的预测性(R > 0.97),但与至少一个检测数据集不一致(p < 10)。≤3μM时的调整后平均反应大致相等(p > 0.30),且超过100%显著(p ≤ 10)。低剂量兴奋效应模型对TS细胞的合并调整后数据拟合最佳(R = 0.995)。(表观HS细胞的比例)估计值存在明显差异,这出乎意料,难以解释,需要使用额外的细胞系和检测方法进行进一步研究。