Altered striosome-matrix distribution and activity of striatal cholinergic interneurons in a model of autism-linked repetitive behaviors

IF 10.1 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jordan Molitor, Juliette Graniou, Pascal Salin, Francis Castets, Ahmed Fatmi, Lydia Kerkerian-Le Goff, Laurent Fasano, Xavier Caubit, Paolo Gubellini
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引用次数: 0

Abstract

Repetitive behaviors are cardinal features of many brain disorders, including autism spectrum disorder (ASD). We previously associated dysfunction of striatal cholinergic interneurons (SCINs) with repetitive behaviors in a mouse model based on conditional deletion of the ASD-related gene Tshz3 in cholinergic neurons (Chat-cKO). Here, we provide evidence linking SCIN abnormalities to the unique organization of the striatum into striosome and matrix compartments, whose imbalances are implicated in several pathological conditions. Chat-cKO mice exhibit an altered relationship between the embryonic birthdate of SCINs and their adult striosome-matrix distribution, leading to an increased proportion of striosomal SCINs. In addition, the ratio of striosomal SCINs with slow-irregular vs. sustained-regular firing is increased, which translates into decreased activity, further stressing the striosome-matrix imbalance. These findings provide novel insights into the pathogenesis of ASD-related stereotyped behaviors by pointing to abnormal developmental compartmentalization and activity of SCINs as a substrate.

Abstract Image

自闭症相关重复行为模型中纹状体基质分布和纹状体胆碱能中间神经元活性的改变
重复行为是许多脑部疾病的主要特征,包括自闭症谱系障碍(ASD)。我们之前在一个基于胆碱能神经元(Chat-cKO)中asd相关基因Tshz3条件缺失的小鼠模型中,将纹状体胆碱能中间神经元(SCINs)功能障碍与重复行为联系起来。在这里,我们提供了证据,将SCIN异常与纹状体的独特组织联系起来,纹状体分为纹状体和基质室,其不平衡与几种病理条件有关。Chat-cKO小鼠显示出SCINs的胚胎出生日期与其成年后的纹状体-基质分布之间的改变关系,导致纹状体SCINs的比例增加。此外,纹状体SCINs缓慢不规则放电与持续规则放电的比例增加,这转化为活性降低,进一步加剧了纹状体-基质的不平衡。这些发现通过指出异常发育区隔化和SCINs活性作为底物,为asd相关刻板行为的发病机制提供了新的见解。
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来源期刊
Molecular Psychiatry
Molecular Psychiatry 医学-精神病学
CiteScore
20.50
自引率
4.50%
发文量
459
审稿时长
4-8 weeks
期刊介绍: Molecular Psychiatry focuses on publishing research that aims to uncover the biological mechanisms behind psychiatric disorders and their treatment. The journal emphasizes studies that bridge pre-clinical and clinical research, covering cellular, molecular, integrative, clinical, imaging, and psychopharmacology levels.
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