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Engrailed 2 缺失的自闭症候选基因小鼠中神经周细胞网表达的改变及异常社会行为和胡须依赖性纹理辨别

Alterations of Perineuronal Net Expression and Abnormal Social Behavior and Whisker-dependent Texture Discrimination in Mice Lacking the Autism Candidate Gene Engrailed 2.

机构信息

Department of Cellular, Computational, and Integrative Biology (CIBIO), University of Trento, via Sommarive 9, 38123 Trento, Italy.

Department of Cellular, Computational, and Integrative Biology (CIBIO), University of Trento, via Sommarive 9, 38123 Trento, Italy.

出版信息

Neuroscience. 2024 May 14;546:63-74. doi: 10.1016/j.neuroscience.2024.03.023. Epub 2024 Mar 25.

DOI:10.1016/j.neuroscience.2024.03.023
PMID:38537894
Abstract

GABAergic interneurons and perineuronal nets (PNNs) are important regulators of plasticity throughout life and their dysfunction has been implicated in the pathogenesis of several neuropsychiatric conditions, including autism spectrum disorders (ASD). PNNs are condensed portions of the extracellular matrix (ECM) that are crucial for neural development and proper formation of synaptic connections. We previously showed a reduced expression of GABAergic interneuron markers in the hippocampus and somatosensory cortex of adult mice lacking the Engrailed2 gene (En2-/- mice), a mouse model of ASD. Since alterations in PNNs have been proposed as a possible pathogenic mechanism in ASD, we hypothesized that the PNN dysfunction may contribute to the neural and behavioral abnormalities of En2-/- mice. Here, we show an increase in the PNN fluorescence intensity, evaluated by Wisteria floribunda agglutinin, in brain regions involved in social behavior and somatosensory processing. In addition, we found that En2-/- mice exhibit altered texture discrimination through whiskers and display a marked decrease in the preference for social novelty. Our results raise the possibility that altered expression of PNNs, together with defects of GABAergic interneurons, might contribute to the pathogenesis of social and sensory behavioral abnormalities.

摘要

GABA 能中间神经元和周围神经网(PNNs)是生命全过程中神经可塑性的重要调节因子,其功能障碍与包括自闭症谱系障碍(ASD)在内的多种神经精神疾病的发病机制有关。PNNs 是细胞外基质(ECM)的浓缩部分,对于神经发育和突触连接的正确形成至关重要。我们之前曾表明,缺乏 Engrailed2 基因(En2-/- 小鼠)的成年小鼠海马体和体感皮层中的 GABA 能中间神经元标志物表达减少,En2-/- 小鼠是 ASD 的一种小鼠模型。由于 PNN 的改变被提出作为 ASD 的一种可能的发病机制,我们假设 PNN 功能障碍可能导致 En2-/- 小鼠的神经和行为异常。在这里,我们通过 Wisteria floribunda agglutinin 评估发现,参与社交行为和体感处理的大脑区域的 PNN 荧光强度增加。此外,我们发现 En2-/- 小鼠通过胡须表现出纹理辨别能力的改变,并显示出对社交新颖性的明显偏好降低。我们的研究结果提出了这样一种可能性,即 PNNs 的表达改变,加上 GABA 能中间神经元的缺陷,可能有助于社交和感觉行为异常的发病机制。

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