Aigner Bernhard
Chair for Molecular Animal Breeding and Biotechnology, LMU Munich, Munich, Germany.
PLoS One. 2025 Aug 7;20(8):e0329357. doi: 10.1371/journal.pone.0329357. eCollection 2025.
The use of mice as animal models in biomedical research allows the standardization of genetic background, housing conditions as well as experimental protocols, which all affect phenotypic variability. In this study, the phenotypic variability of test parameters was analyzed in genetically identical mice of different age groups, i.e., early adults versus late adults. Therefore, published data sets of genetically identical mice of different age groups collected from the same investigator/ project were retrospectively analyzed. Morphological parameters, blood parameters and behavioral tests were analyzed which are predominantly used in biomedical research. The JaxKOMP project examined C57BL/6NJ mice with an age of 7-20 weeks and 66-81 weeks. Further substrains of C57BL/6N mice with an age of 8-16 weeks and 49-63 weeks were examined as wild-type controls from various investigators of the International Mouse Phenotyping Consortium (IMPC). Additional data sets of young and old groups of genetically identical mice were derived from the Mouse Phenome Database (MPD) and the RIKEN BioResource Research Center (RBRC). The phenotypic variability of the chosen traits and parameters was measured by calculating the coefficient of variation (CV = standard deviation/ mean) of the animals with the same sex of a given mouse strain. Subsequently, the CVs of the young and the old mouse group were compared. The comparison of the phenotypic variability of the late adults versus early adults revealed the appearance of unpredictable interactions between genotype, environment and experiment. Overall, a higher phenotypic variability of the late adults appeared almost consistently for body weight including lean mass and fat mass for females as well as for hematology and immunology parameters, particularly for females. Clinical chemistry often appeared inconspicuous. No noticeable differences were detected for the traits echocardiography and electrocardiogram, whereas late adults also often showed a higher phenotypic variability for behavioral tests.
在生物医学研究中使用小鼠作为动物模型,可以使遗传背景、饲养条件以及实验方案标准化,而这些因素都会影响表型变异性。在本研究中,对不同年龄组(即成年早期与成年晚期)的基因相同的小鼠的测试参数的表型变异性进行了分析。因此,回顾性分析了从同一研究者/项目收集的不同年龄组的基因相同的小鼠的已发表数据集。分析了生物医学研究中主要使用的形态学参数、血液参数和行为测试。JaxKOMP项目研究了7至20周龄和66至81周龄的C57BL/6NJ小鼠。作为国际小鼠表型分析联盟(IMPC)各研究者提供的野生型对照,还研究了8至16周龄和49至63周龄的C57BL/6N小鼠的其他亚系。基因相同的小鼠的年轻和老年组的其他数据集来自小鼠表型数据库(MPD)和理化学研究所生物资源研究中心(RBRC)。通过计算给定小鼠品系相同性别的动物的变异系数(CV =标准差/平均值)来测量所选性状和参数的表型变异性。随后,比较了年轻和老年小鼠组的CV。成年晚期与成年早期的表型变异性比较揭示了基因型、环境和实验之间不可预测的相互作用的出现。总体而言,成年晚期在体重(包括雌性的瘦体重和脂肪量)以及血液学和免疫学参数(特别是雌性)方面几乎始终表现出较高的表型变异性。临床化学通常不明显。在超声心动图和心电图性状方面未检测到明显差异,而成年晚期在行为测试中也经常表现出较高的表型变异性。