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首页> 外文期刊>Mammalian genome: official journal of the International Mammalian Genome Society >Differences in bone structure and unloading-induced bone loss between C57BL/6N and C57BL/6J mice
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Differences in bone structure and unloading-induced bone loss between C57BL/6N and C57BL/6J mice

机译:骨结构和卸载诱导的C57BL / 6N和C57BL / 6J小鼠之间的骨质损失的差异

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The C57BL/6 mouse, the most frequently utilized animal model in biomedical research, is in use as several substrains, all of which differ by a small array of genomic differences. Two of these substrains, C57BL/6J (B6J) and C57BL/6N (B6N), are commonly used but it is unclear how phenotypically similar or different they are. Here, we tested whether adolescent B6N mice have a bone phenotype and respond to the loss of weightbearing differently than B6J. At 9 weeks of age, normally ambulating B6N had lower trabecular bone volume fraction but greater bone formation rates and osteoblast surfaces than corresponding B6J. At 11 weeks of age, differences in trabecular indices persisted between the substrains but differences in cellular activity had ceased. Cortical bone indices were largely similar between the two substrains. Hindlimb unloading (HLU) induced similar degeneration of trabecular architecture and cellular activity in both substrains when comparing 11-week-old HLU mice to 11-week-old controls. However, unloaded B6N mice had smaller cortices than B6J. When comparing HLU to 9 weeks baseline control mice, deterioration in trabecular separation, osteoblast indices, and endocortical variables was significantly greater in B6N than B6J. These data indicate specific developmental differences in bone formation and morphology between B6N and B6J mice, giving rise to a differential response to mechanical unloading that may be modulated, in part, by the genes Herc2, Myo18b, and Acan. Our results emphasize that these substrains cannot be used interchangeably at least for investigations in which the phenotypic makeup and its response to extraneous stimuli are of interest.
机译:C57BL / 6鼠标是生物医学研究中最常利用的动物模型,在使用的几个基因中,所有这些都会因小阵列的基因组差异而异。这些底端中的两个,C57BL / 6J(B6J)和C57BL / 6N(B6N)通常使用,但目前尚不清楚如何相似或不同的方式。在这里,我们测试了青少年B6N小鼠是否具有骨表型并响应超重的丧失而不是B6J。在9周龄时,通常小梁B6N具有较低的小梁骨体积分数,但比相应的B6J更高的骨形成率和成骨细胞表面。在11周龄时,缺乏细胞活动的缺陷症仍然存在的小梁索引的差异已停止。两个底板之间皮质骨指数在很大程度上相似。当将11周龄HLU小鼠与11周龄对照组进行比较时,后肢卸载(HLU)诱导在两种亚颌下中的小梁架构和细胞活性的类似退化。然而,卸载的B6N小鼠具有比B6J更小的皮质。当将Hlu到9周的基线对照小鼠比较时,B6N比B6J在B6N中劣化,骨细胞指数和内蚀变量的劣化显着更大。这些数据表明B6N和B6J小鼠之间的骨形成和形态的特异性发育差异,从而对机械卸载产生差异响应,其可以部分地由基因植物2,MyO18B和Acan调节。我们的结果强调,这些亚底具有至少用于调查的这些底物不能互换使用,其中表型化妆及其对外来刺激的反应是感兴趣的。

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