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雄性和雌性基因敲除小鼠的行为、神经递质和转录组分析。

Behavioral, neurotransmitter and transcriptomic analyses in male and female KO mice.

作者信息

McCarthy Deirdre M, Vied Cynthia, Trupiano Mia X, Canekeratne Angeli J, Wang Yuan, Schatschneider Christopher, Bhide Pradeep G

机构信息

Department of Biomedical Sciences, Florida State University College of Medicine, Tallahassee, FL, United States.

Center for Brain Repair, Florida State University College of Medicine, Tallahassee, FL, United States.

出版信息

Front Behav Neurosci. 2024 Sep 6;18:1458502. doi: 10.3389/fnbeh.2024.1458502. eCollection 2024.

Abstract

INTRODUCTION

Fragile X syndrome is an inherited X-linked disorder associated with intellectual disabilities that begin in childhood and last a lifetime. The symptoms overlap with autism spectrum disorder, and the syndrome predominantly affects males. Consequently, FXS research tends to favor analysis of social behaviors in males, leaving a gap in our understanding of other behavioral traits, especially in females.

METHODS

We used a mouse model of FXS to analyze developmental, behavioral, neurochemical, and transcriptomic profiles in males and females.

RESULTS

Our behavioral assays demonstrated locomotor hyperactivity, motor impulsivity, increased "approach" behavior in an approach-avoidance assay, and deficits in nest building behavior. Analysis of brain neurotransmitter content revealed deficits in striatal GABA, glutamate, and serotonin content. RNA sequencing of the ventral striatum unveiled expression changes associated with neurotransmission as well as motivation and substance use pathways. Sex differences were identified in nest building behavior, striatal neurotransmitter content, and ventral striatal gene expression.

DISCUSSION

In summary, our study identified sex differences in specific behavioral, neurotransmitter, and gene expression phenotypes and gene set enrichment analysis identified significant enrichment of pathways associated with motivation and drug reward.

摘要

引言

脆性X综合征是一种遗传性X连锁疾病,与始于儿童期并持续终生的智力残疾有关。其症状与自闭症谱系障碍重叠,且该综合征主要影响男性。因此,脆性X综合征的研究倾向于对男性的社会行为进行分析,这使得我们对其他行为特征的理解存在空白,尤其是在女性方面。

方法

我们使用脆性X综合征的小鼠模型来分析雄性和雌性小鼠的发育、行为、神经化学和转录组特征。

结果

我们的行为分析表明,小鼠存在运动活动亢进、运动冲动性、在趋避试验中“趋近”行为增加以及筑巢行为缺陷。对脑神经递质含量的分析显示,纹状体中γ-氨基丁酸、谷氨酸和血清素含量存在缺陷。腹侧纹状体的RNA测序揭示了与神经传递以及动机和物质使用途径相关的表达变化。在筑巢行为、纹状体神经递质含量和腹侧纹状体基因表达方面发现了性别差异。

讨论

总之,我们的研究确定了特定行为、神经递质和基因表达表型中的性别差异,并且基因集富集分析确定了与动机和药物奖赏相关途径的显著富集。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/901a/11412825/e38af021850f/fnbeh-18-1458502-g001.jpg

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