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补体在16p11.2半缺失小鼠模型中导致多动行为。

Complement contributes to hyperactive behavior in the 16p11.2 hemideletion mouse model.

作者信息

Kelvington Benjamin A, Kim Jaekyoon, Fair Regan, Gaine Marie E, Abel Ted

机构信息

Department of Neuroscience and Pharmacology, Carver College of Medicine, University of Iowa.

Iowa Neuroscience Institute, University of Iowa.

出版信息

bioRxiv. 2025 Aug 21:2025.08.21.671537. doi: 10.1101/2025.08.21.671537.

Abstract

The complement system is a major component of the innate immune system and plays an important role in immune surveillance. Recent research has demonstrated that the complement system also plays pivotal roles in brain development, and dysregulation of complement is involved in neurodegenerative and neuropsychiatric disorders. However, the mechanisms by which the complement system contributes to neurodevelopmental disorders (NDDs) remain poorly understood. In this study, we find that the expression of a central regulator of the complement cascade, complement component 3 (C3), is upregulated in the striatum of mice modeling the 16p11.2 hemideletion (16p11.2 del). 16p11.2 del is among the most common copy number variations associated with NDDs including attention deficit hyperactivity disorder (ADHD), autism spectrum disorder (ASD), and intellectual disability (ID). Pharmacological inhibition of the C3a receptor alleviates hyperactivity in 16p11.2 del mice, suggesting that elevated complement contributes to NDD-relevant behavioral changes. Due to the pro-inflammatory actions of the C3a receptor, we assess the cytokine environment in the striatum, a key neural substrate for locomotor behavior, and find that several inflammatory factors are upregulated in 16p11.2 del mice. Collectively, these results indicate that increased expression of the complement system, especially C3, mediates hyperactive behavior and is associated with a pro-inflammatory environment in the striatum of 16p11.2 del mice. Our results suggest that inhibition of an overactive complement system may be an effective strategy to ameliorate NDD symptoms resulting from 16p11.2 hemideletion including those associated with ADHD.

摘要

补体系统是固有免疫系统的主要组成部分,在免疫监视中发挥重要作用。最近的研究表明,补体系统在大脑发育中也起着关键作用,补体失调与神经退行性疾病和神经精神疾病有关。然而,补体系统导致神经发育障碍(NDDs)的机制仍知之甚少。在本研究中,我们发现补体级联反应的核心调节因子补体成分3(C3)在模拟16p11.2半缺失(16p11.2 del)的小鼠纹状体中表达上调。16p11.2 del是与NDDs相关的最常见拷贝数变异之一,包括注意力缺陷多动障碍(ADHD)、自闭症谱系障碍(ASD)和智力残疾(ID)。对C3a受体的药理抑制可减轻16p11.2 del小鼠的多动症状,这表明补体升高会导致与NDD相关的行为变化。由于C3a受体的促炎作用,我们评估了纹状体(运动行为的关键神经底物)中的细胞因子环境,发现16p11.2 del小鼠中几种炎症因子上调。总体而言,这些结果表明补体系统,尤其是C3的表达增加介导了多动行为,并与16p11.2 del小鼠纹状体中的促炎环境有关。我们的结果表明,抑制过度活跃的补体系统可能是改善由16p11.2半缺失引起的NDD症状(包括与ADHD相关的症状)的有效策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c240/12393526/1df71863ab8d/nihpp-2025.08.21.671537v1-f0001.jpg

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