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正在孵卵的雌性树燕应对社会挑战及产生母性攻击行为时的大脑转录组学研究

Brain transcriptomics of a social challenge and maternal aggression in incubating female tree swallows.

作者信息

Levy Emily J, George Elizabeth M, Rusch Douglas B, Buechlein Aaron, Rosvall Kimberly A

机构信息

Indiana University Bloomington, Department of Biology, 1001 E 3rd St, Bloomington, IN 47405, United States of America; Sacred Heart University, Biology Department, 5151 Park Ave, Fairfield, CT 06825, United States of America.

Indiana University Bloomington, Department of Biology, 1001 E 3rd St, Bloomington, IN 47405, United States of America; The Ohio State University, Department of Evolution, Ecology and Organismal Biology, 300 Aronoff Laboratory, 318 W 12th Ave, Columbus, OH 43210, United States of America.

出版信息

Horm Behav. 2025 Feb;168:105692. doi: 10.1016/j.yhbeh.2025.105692. Epub 2025 Feb 1.

DOI:10.1016/j.yhbeh.2025.105692
PMID:39893820
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11892343/
Abstract

Aggressive behavior is ubiquitous across many contexts, including defense of territories, mates, and offspring. For decades, researchers have detailed the effect of aggressive behavior on physiology, but our understanding of these mechanisms in females lags behind that of males, despite the fact that female aggression is widespread, particularly in the context of maternal defense of eggs or offspring (i.e., maternal aggression). Here, we measured effects of a social challenge on brain gene expression in free-living incubating females. We hypothesized that the social challenge would generate at least one of three transcriptomic effects: (1) sensitizing the brain to otherwise low levels of sex steroids, (2) changing other neuroendocrine signaling pathways associated with social behavior (e.g., dopamine), or (3) broad shifts related to metabolism or immune function. We tested these hypotheses in incubating female tree swallows (Tachycineta bicolor), exposing 10 females to a 30-min simulated territorial intrusion, which elicited maternal aggression. After this challenge, we measured neural gene expression via RNA-seq and compared gene expression to 10 unchallenged controls. We saw no global treatment effect on gene expression. However, within the experimental group, more maternal aggression was correlated with upregulation of genes associated with immune activation and downregulation of genes associated with synaptic plasticity. Though more research is needed to understand the downstream effects of these transcriptional differences, our findings generate key questions about how the brain responds to social challenges across different contexts.

摘要

攻击性行为在许多情境中普遍存在,包括对领地、配偶和后代的防御。几十年来,研究人员详细阐述了攻击性行为对生理的影响,但我们对雌性动物这些机制的理解落后于雄性,尽管雌性攻击行为很普遍,特别是在对卵或后代进行母性防御的情境中(即母性攻击)。在此,我们测量了社会挑战对自由生活的正在孵卵的雌性动物大脑基因表达的影响。我们假设这种社会挑战会产生三种转录组效应中的至少一种:(1)使大脑对原本低水平的性类固醇敏感,(2)改变与社会行为相关的其他神经内分泌信号通路(如多巴胺),或(3)与新陈代谢或免疫功能相关的广泛变化。我们在正在孵卵的雌性双色树燕中检验了这些假设,让10只雌性树燕暴露于30分钟的模拟领地入侵中,这引发了母性攻击。在这种挑战之后,我们通过RNA测序测量神经基因表达,并将基因表达与10只未受挑战的对照进行比较。我们没有看到对基因表达的整体处理效应。然而,在实验组中,更多的母性攻击与免疫激活相关基因的上调以及与突触可塑性相关基因的下调相关。尽管需要更多研究来了解这些转录差异的下游效应,但我们的发现提出了关于大脑如何在不同情境下对社会挑战做出反应的关键问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f6/11892343/e5e7d8b28d7b/nihms-2054227-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f6/11892343/3894f196d77c/nihms-2054227-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f6/11892343/2368b51539b5/nihms-2054227-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f6/11892343/24dde8e7b087/nihms-2054227-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f6/11892343/1b92a4f521d9/nihms-2054227-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f6/11892343/e5e7d8b28d7b/nihms-2054227-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f6/11892343/3894f196d77c/nihms-2054227-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f6/11892343/2368b51539b5/nihms-2054227-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f6/11892343/24dde8e7b087/nihms-2054227-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f6/11892343/1b92a4f521d9/nihms-2054227-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f6/11892343/e5e7d8b28d7b/nihms-2054227-f0005.jpg

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本文引用的文献

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A female-biased gene expression signature of dominance in cooperatively breeding meerkats.合作繁殖的猫鼬中支配地位的雌性偏倚基因表达特征。
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Associations of the immune system in aggression traits and the role of microglia as mediators.免疫系统与攻击特质的关联以及小胶质细胞作为中介的作用。
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An Aggressive Interaction Rapidly Increases Brain Androgens in a Male Songbird during the Non-breeding Season.
在非繁殖季节,雄性鸣禽中具有攻击性的互动会迅速增加大脑中的雄激素。
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