Whole-Brain Mapping of Neuronal Activity Associated with Vocal Socialization Behaviors in Adult Mice.

IF 2.7 3区 医学 Q3 NEUROSCIENCES
eNeuro Pub Date : 2026-05-06 DOI:10.1523/ENEURO.0400-25.2026
Shi-Xiang Luo, Shih-Yun Chen, Hsiao-Ying Kuo, Fu-Chin Liu
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引用次数: 0

Abstract

Vocal communication is essential for social behavior, yet the distributed brain networks underlying vocal production remain elusive. Male mice produce ultrasonic vocalizations (USVs) during courtship, providing a rodent model for investigating neural circuits underlying innate vocal communication. Here, we used a double-labelling strategy that combined genetic activity tagging (TRAP2) and c-Fos immunohistochemistry to generate an unbiased, whole-brain map of neuronal ensembles activated during courtship-induced USV production in adult male mice. By tracking neuronal activity across 25 brain regions during two independent courtship sessions, we identified populations consistently recruited during social vocalization. Quantitative analyses revealed robust activation in the caudal periaqueductal gray, confirming its established role as a hub for vocal motor control. Importantly, correlation analyses between neuronal activity and USV count distinguished regions specifically linked to vocal output from those associated with general social interaction. The medial prefrontal cortex, particularly the prelimbic and cingulate cortices, exhibited strong positive correlations with USV production, suggesting an integrative role in translating the social and motivational context into vocal commands. Notably, the rostral striatum showed a strong correlation with USV count, with vocalization-related activity preferentially localized within striosome compartments of the medial striatum. Given that striosomes receive limbic cortical input and are implicated in motivational processing, these findings suggest that corticostriatal limbic-motor circuits modulate innate vocalization contingent on emotional and social contexts. Collectively, our study proposes a comprehensive neuroanatomical framework linking cortical motivation centers, striatal limbic-motor pathways, and brainstem vocal motor circuits, providing insights into the distributed neural architecture underlying mammalian social communication.Significance Statement Mouse ultrasonic vocalizations (USVs) provide a mammalian model for investigating the neural circuits underlying social communication. Using whole-brain activity mapping with double labeling of TRAP2 and c-Fos, we identified a distributed network extending from the medial prefrontal cortex and striatum to the periaqueductal gray that is recruited during courtship-induced vocalization. The discovery that USV-related neurons in the striatum are preferentially localized to striosomal compartments reveals a potential limbic-motor interface for integrating social motivation with vocal motor output. Together, these findings identify a multi-level neural network that may be evolutionarily conserved for integrating motivation and motor control in mammalian communication.

与成年小鼠发声社会化行为相关的神经元活动的全脑图谱。
声音交流对社会行为至关重要,然而,声音产生背后的分布式大脑网络仍然难以捉摸。雄性小鼠在求偶期间产生超声波发声(usv),为研究先天声音交流背后的神经回路提供了一种啮齿动物模型。在这里,我们使用了双重标记策略,结合了遗传活性标记(TRAP2)和c-Fos免疫组织化学,在成年雄性小鼠求爱诱导的USV产生过程中生成了一个无偏倚的全脑神经元集合图。通过在两个独立的求爱过程中跟踪25个大脑区域的神经元活动,我们确定了在社会发声过程中持续招募的人群。定量分析显示尾侧导水管周围灰质活跃,证实了其作为声音运动控制中枢的既定作用。重要的是,神经元活动和USV计数之间的相关性分析区分了与声音输出相关的区域和与一般社会互动相关的区域。内侧前额叶皮层,特别是前边缘和扣带皮层,与USV的产生表现出强烈的正相关,这表明在将社会和动机背景转化为声音命令方面具有综合作用。值得注意的是,吻侧纹状体与USV计数有很强的相关性,与发声相关的活动优先定位于内侧纹状体的纹状体室。考虑到纹状体接受边缘皮质输入并参与动机加工,这些发现表明皮质纹状体边缘运动回路调节基于情感和社会背景的先天发声。总的来说,我们的研究提出了一个综合的神经解剖学框架,连接皮层动机中心,纹状体边缘运动通路和脑干发声运动回路,为哺乳动物社会交流的分布式神经结构提供了见解。小鼠超声发声(usv)为研究社会交流的神经回路提供了一种哺乳动物模型。利用TRAP2和c-Fos双标记的全脑活动图谱,我们发现了一个分布网络,从内侧前额叶皮层和纹状体延伸到导水管周围灰质,该网络在求爱诱导的发声过程中被招募。纹状体中与usv相关的神经元优先定位于纹状体室的发现揭示了将社会动机与发声运动输出相结合的潜在边缘-运动界面。总之,这些发现确定了一个多层次的神经网络,它可能在进化上保守地整合了哺乳动物交流中的动机和运动控制。
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来源期刊
eNeuro
eNeuro Neuroscience-General Neuroscience
CiteScore
5.00
自引率
2.90%
发文量
486
审稿时长
16 weeks
期刊介绍: An open-access journal from the Society for Neuroscience, eNeuro publishes high-quality, broad-based, peer-reviewed research focused solely on the field of neuroscience. eNeuro embodies an emerging scientific vision that offers a new experience for authors and readers, all in support of the Society’s mission to advance understanding of the brain and nervous system.
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