Molitor Jordan, Graniou Juliette, Salin Pascal, Castets Francis, Fatmi Ahmed, Kerkerian-Le Goff Lydia, Fasano Laurent, Caubit Xavier, Gubellini Paolo
Aix-Marseille Univ, CNRS, IBDM, UMR7288, Marseille, France.
Aix-Marseille Univ, CNRS, CRPN, UMR7077, Marseille, France.
Mol Psychiatry. 2025 Sep 5. doi: 10.1038/s41380-025-03208-5.
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.
重复行为是包括自闭症谱系障碍(ASD)在内的许多脑部疾病的主要特征。我们之前在一个小鼠模型中,基于条件性敲除胆碱能神经元中与ASD相关的基因Tshz3(Chat-cKO),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。在此,我们提供证据表明,SCIN异常与纹状体独特地组织为纹状体小体和基质区室有关,这些区室的失衡与多种病理状况有关。Chat-cKO小鼠表现出SCINs的胚胎出生日期与其成年纹状体小体-基质分布之间的关系改变,导致纹状体小体SCINs的比例增加。此外,具有慢不规则放电与持续规则放电的纹状体小体SCINs的比例增加,这转化为活性降低,进一步凸显了纹状体小体-基质失衡。这些发现通过指出SCINs异常的发育区室化和活性作为一种基础,为ASD相关刻板行为的发病机制提供了新的见解。