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神经连接蛋白1通过调节表达纹状体D2受体的中型多棘神经元的活性来调控自闭症样重复行为。

Neuroligin 1 Regulates Autistic-Like Repetitive Behavior through Modulating the Activity of Striatal D2 Receptor-Expressing Medium Spiny Neurons.

作者信息

Lv Dandan, Liu An, Yi Ziyue, Mu Mingdao, Wu Miao, Li Xingcan, Cao Kun, Liu Ruining, Jia Zhengping, Han Junhai, Xie Wei

机构信息

The Key Laboratory of Developmental Genes and Human Disease, The School of Life Science and Technology, Southeast University, 2 Sipailou Road, Nanjing, 210096, China.

Institute for Brain and Intelligence, Southeast University, 2 Sipailou Road, Nanjing, 210096, China.

出版信息

Adv Sci (Weinh). 2025 Feb;12(5):e2410728. doi: 10.1002/advs.202410728. Epub 2024 Dec 11.

Abstract

Restricted and repetitive behavior (RRB) is a primary symptom of autism spectrum disorder (ASD), which poses a significant risk to individuals' health and is becoming increasingly prevalent. However, the specific cellular and neural circuit mechanisms underlying the generation of RRB remain unclear. In this study, it is reported that the absence of the ASD-related protein Neuroligin 1 (NLGN1) in dopamine receptor D2-expressing medium spiny neurons (D2-MSNs) in the dorsal striatum is associated with the duration and frequency of self-grooming and digging behaviors. The Nlgn1-deficient D2-MSNs are hyperactivated, which correlates with excessive self-grooming and digging behaviors. Inhibiting the activity of D2-MSNs reduces the duration and frequency of these RRBs. Furthermore, it is demonstrated that the generation of self-grooming and digging behaviors depends on distinct patterns of D2-MSN activity. Finally, through single-nucleus RNA sequencing (sn-RNAseq) and protein detection verification, it is revealed that the overactivation of protein kinase C (PKC) in Nlgn1-deficient mice contributes to excessive repetitive behaviors and increased neuronal excitability. In this study, potential mechanisms are proposed for the generation of self-grooming and digging behaviors, as well as suggest possible treatments and interventions ASD.

摘要

受限及重复行为(RRB)是自闭症谱系障碍(ASD)的主要症状,对个体健康构成重大风险且愈发普遍。然而,RRB产生的具体细胞及神经回路机制仍不清楚。在本研究中,有报道称背侧纹状体中表达多巴胺受体D2的中型多棘神经元(D2-MSNs)中缺乏自闭症谱系障碍相关蛋白神经连接蛋白1(NLGN1)与自我梳理和挖掘行为的持续时间及频率有关。Nlgn1基因缺陷的D2-MSNs过度激活,这与过度的自我梳理和挖掘行为相关。抑制D2-MSNs的活性可减少这些RRB的持续时间和频率。此外,研究表明自我梳理和挖掘行为的产生取决于D2-MSNs不同的活动模式。最后,通过单核RNA测序(sn-RNAseq)和蛋白质检测验证,发现Nlgn1基因缺陷小鼠中蛋白激酶C(PKC)的过度激活导致了过度的重复行为和神经元兴奋性增加。在本研究中,提出了自我梳理和挖掘行为产生的潜在机制,并为自闭症谱系障碍提出了可能的治疗和干预建议。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f90/11792054/99bb5ef83d58/ADVS-12-2410728-g007.jpg

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