Sex differences in structural and receptor mRNA expression in the ventral anterior cingulate cortex and a potential role of perineuronal nets in monogamous pair bond establishment (Peromyscus californicus).

IF 5.1 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Candice L Malone, Jiaxuan Li, Elsa M Luebke, Leykza Carreras-Simons, Warren W Treis, Emma R Hammond, Patrick K Monari, Catherine A Marler
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Abstract

The monogamous California mouse (Peromyscus californicus) exhibits distinct behavioral changes during pair bond formation. Using a detailed temporal behavioral analysis over seven days, we found a rapid decrease in aggression within 24 h of pair introduction in this highly territorial species. After this aggression reduction, the gradual increase in affiliative behaviors varied by type of affiliative behavior and ranged from one to seven days. We then measured neurobiological changes at three time points during this transition to uncover mechanisms that might govern this shift from aggressive to affiliative behavior, revealing novel sex differences that add to current research on biological mechanisms of social bonding. Specifically, we examined plasticity through mRNA expression of two perineuronal net (PNN) associated proteins, HAPLN and ACAN, in two brain regions implicated in affiliation, aggression, and social cognition: the ventral anterior cingulate cortex (vACC) and lateral septum (LS). The vACC in females exhibited higher expression levels of both of these PNN components relative to males. Additionally, we observed a decrease in ACAN mRNA expression in the vACC over the course of pair bond establishment, but no such change in the LS. Furthermore, oxytocin receptor (OXTR) and vasopressin receptor (AVPR) plasticity exhibited sex-specific patterns in the vACC during pair bond formation. Females displayed higher OXTR mRNA expression across the bonding period, whereas males expressed higher AVPR mRNA levels. We discuss how a decrease in PNNs could allow for an increase in receptor plasticity in the vACC as the pair bond is established. Moreover, we suggest that structural plasticity across this social transition may differ between males and females due to factors such as pre-pair sociality and aggression/territoriality changes.

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腹侧前扣带皮层结构和受体mRNA表达的性别差异以及神经元周围网络在一夫一妻制配对建立中的潜在作用(加利福尼亚细骨肌)。
一夫一妻制的加利福尼亚鼠(Peromyscus californicus)在配对形成过程中表现出明显的行为变化。通过对7天的详细时间行为分析,我们发现在配对引入后的24小时内,这种高度领地性的物种的攻击行为迅速下降。在攻击减少之后,随着亲近行为类型的不同,亲近行为的逐渐增加从1天到7天不等。然后,我们测量了这一转变过程中三个时间点的神经生物学变化,以揭示可能导致这种从攻击性行为向附属行为转变的机制,揭示了新的性别差异,为目前关于社会联系生物学机制的研究增添了新的内容。具体来说,我们通过两种与神经网络(PNN)相关的蛋白,HAPLN和ACAN的mRNA表达来检测可塑性,这两种蛋白在两个涉及联系、攻击和社会认知的大脑区域:腹侧前扣带皮层(vACC)和外侧隔(LS)。与男性相比,女性的vACC中这两种PNN成分的表达水平更高。此外,我们观察到ACAN mRNA在vACC中的表达在配对键建立过程中下降,但在LS中没有这种变化。此外,催产素受体(OXTR)和抗利尿激素受体(AVPR)的可塑性在配对键形成过程中表现出性别特异性模式。雌性在整个结合期间表现出较高的OXTR mRNA表达,而雄性则表现出较高的AVPR mRNA水平。我们讨论了pnn的减少如何允许vACC中受体可塑性的增加,因为偶键是建立的。此外,我们认为在这种社会转变过程中,男性和女性的结构可塑性可能因配对前社会性和侵略/领土变化等因素而有所不同。
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来源期刊
Biology of Sex Differences
Biology of Sex Differences ENDOCRINOLOGY & METABOLISM-GENETICS & HEREDITY
CiteScore
12.10
自引率
1.30%
发文量
69
审稿时长
14 weeks
期刊介绍: Biology of Sex Differences is a unique scientific journal focusing on sex differences in physiology, behavior, and disease from molecular to phenotypic levels, incorporating both basic and clinical research. The journal aims to enhance understanding of basic principles and facilitate the development of therapeutic and diagnostic tools specific to sex differences. As an open-access journal, it is the official publication of the Organization for the Study of Sex Differences and co-published by the Society for Women's Health Research. Topical areas include, but are not limited to sex differences in: genomics; the microbiome; epigenetics; molecular and cell biology; tissue biology; physiology; interaction of tissue systems, in any system including adipose, behavioral, cardiovascular, immune, muscular, neural, renal, and skeletal; clinical studies bearing on sex differences in disease or response to therapy.
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