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Distinct inflammatory and transcriptomic profiles in dominant versus subordinate males in mouse social hierarchies
bioRxiv - Immunology Pub Date : 2021-09-06 , DOI: 10.1101/2021.09.04.458987
Won Lee , Tyler Marie Milewski , Madeleine F Dwortz , Rebecca L Young , Andrew D Gaudet , Laura K Fonken , Frances A Champagne , James P Curley

Social status is a critical factor determining health outcomes in human and nonhuman social species. In social hierarchies with reproductive skew, individuals compete to monopolize resources and increase mating opportunities. This can come at a significant energetic cost leading to trade-offs between different physiological systems. Particularly, changes in energetic investment in the immune system can have significant short and long-term effects on fitness and health. We have previously found that dominant alpha male mice living in social hierarchies have increased metabolic demands related to territorial defense. In this study, we tested the hypothesis that high-ranking male mice favor energetically inexpensive adaptive immunity, while subordinate mice show higher investment in innate immunity. We housed 12 groups of 10 outbred CD-1 male mice in a social housing system. All formed linear social hierarchies and subordinate mice had higher concentrations of plasma corticosterone (CORT) than alpha males. This difference was heightened in highly despotic hierarchies. Using flow cytometry, we found that dominant status was associated with a significant shift in immunophenotypes towards favoring adaptive versus innate immunity. Using Tag-Seq to profile hepatic and splenic transcriptomes of alpha and subordinate males, we identified genes that regulate metabolic and immune defense pathways that are associated with status and/or CORT concentration. In the liver, dominant animals showed an up-regulation of specific genes involved in major urinary production and catabolic processes, whereas subordinate animals showed an up-regulation of genes promoting biosynthetic processes, wound healing, and proinflammatory responses. In spleen, subordinate mice showed up-regulation of genes facilitating oxidative phosphorylation and DNA repair and CORT was negatively associated with genes involved in lymphocyte proliferation and activation. Together, our findings suggest that dominant and subordinate animals adaptively shift energy investment in immune functioning and gene expression to match their contextual energetic demands.

中文翻译:

小鼠社会等级中优势雄性与从属雄性的不同炎症和转录组学特征

社会地位是决定人类和非人类社会物种健康结果的关键因素。在具有生殖倾斜的社会等级制度中,个体竞争以垄断资源并增加交配机会。这可能会带来巨大的能量成本,导致不同生理系统之间的权衡。特别是,免疫系统能量投入的变化会对健身和健康产生显着的短期和长期影响。我们之前已经发现,生活在社会等级制度中的占主导地位的 alpha 雄性小鼠增加了与领土防御相关的代谢需求。在这项研究中,我们检验了这样一个假设,即高级雄性小鼠喜欢精力充沛的廉价适应性免疫,而下属小鼠对先天免疫表现出更高的投资。我们在社会住房系统中安置了 12 组 10 只远交 CD-1 雄性小鼠。所有形成的线性社会等级和下属小鼠的血浆皮质酮 (CORT) 浓度都高于 alpha 雄性。这种差异在高度专制的等级制度中更加突出。使用流式细胞术,我们发现显性状态与免疫表型向有利于适应性免疫与先天免疫的显着转变有关。使用 Tag-Seq 分析 alpha 和下属男性的肝脏和脾脏转录组,我们确定了调节与状态和/或 CORT 浓度相关的代谢和免疫防御途径的基因。在肝脏中,显性动物表现出参与主要尿液产生和分解代谢过程的特定基因的上调,而下属动物则显示出促进生物合成过程、伤口愈合和促炎反应的基因上调。在脾脏中,下属小鼠显示出促进氧化磷酸化和 DNA 修复的基因上调,并且 CORT 与参与淋巴细胞增殖和激活的基因呈负相关。总之,我们的研究结果表明,优势动物和从属动物会适应性地转移对免疫功能和基因表达的能量投资,以匹配其环境能量需求。
更新日期:2021-09-10
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