Chair for Molecular Animal Breeding and Biotechnology, and Laboratory for Functional Genome Analysis (LAFUGA), Gene Center, LMU Munich, Munich, Germany.
Physiol Res. 2021 Apr 30;70(2):227-236. doi: 10.33549/physiolres.934577. Epub 2021 Mar 8.
Mice are important models for biomedical research by providing the possibility of standardizing genetic background and environmental conditions, which both affect phenotypic variability. Use of both sexes in experiments is strongly recommended because of possible differences in the outcome. However, sex-specific phenotypic variability is discussed with regard to putative consequences on the group size which is necessary for achieving valid and reproducible results. Here, we retrospectively analyzed the sex-specific variability of 25 blood parameters of C3H inbred mice in two different mouse facilities withinthe long-term, high-throughput Munich ENU mouse mutagenesis project. Using the 95 % data range, data of4,780-20,706 mice per parameter were analyzed and resulted in ratios of the coefficient of variation (= female CV / (female CV + male CV)) from 0.44 to 0.58 for the 25 parameters, with an overall mean of 0.51 in both facilities. Together with data analyses of three additional, smaller studies with 72-247 animals per parameter examined and various genetic backgrounds (inbred strains, F1 hybrids) included, hints for reproducible sex-specific variability were observed for particular parameters. Thus, the overall analysis comprising all 25 clinical chemical and hematological parameters of the standardized, long-term analysis of a high number of group housed, young adult, twelve-week-old C3H inbred mice showed no evidence for substantial sex-specific variability. The results may provide a basis for the examination of sex-specific variability in particular blood parameters.
小鼠是生物医学研究的重要模型,因为它们提供了标准化遗传背景和环境条件的可能性,而这些因素都会影响表型的可变性。强烈建议在实验中同时使用雌雄两种性别,因为性别可能会对结果产生影响。然而,我们需要讨论的是,由于组大小对获得有效且可重复的结果的必要性,可能会导致表型的性别特异性变化。在这里,我们回顾性地分析了 25 个血液参数在两个不同的小鼠设施中 C3H 近交系小鼠的性别特异性变异性,这两个设施都参与了长期、高通量的慕尼黑ENU 小鼠诱变项目。使用 95%的数据范围,对每个参数的 4780-20706 只小鼠的数据进行了分析,结果得出的系数变异比(=雌性 CV /(雌性 CV + 雄性 CV))在 25 个参数中从 0.44 到 0.58,两个设施的总体平均值均为 0.51。此外,对另外三个规模较小的研究的数据进行了分析,每个研究的动物数量为 72-247 只,包括不同的遗传背景(近交系、F1 杂交),观察到了一些特定参数的可重复性别特异性变异性的迹象。因此,对包含所有 25 个临床化学和血液学参数的长期标准化分析,对大量群体饲养的年轻成年 12 周龄 C3H 近交系小鼠进行的综合分析,并未发现显著的性别特异性变异性。这些结果可能为特定血液参数的性别特异性变异性的研究提供了依据。