Leibniz-Forschungsinstitut für Molekulare Pharmakologie, 13125 Berlin, Germany.
Department of Nanophysiology, Faculty of Biology, Rheinland-Pfälzische Technische Universität Kaiserslautern-Landau, 67663 Kaiserslautern, Germany.
Proc Natl Acad Sci U S A. 2023 Aug 29;120(35):e2304323120. doi: 10.1073/pnas.2304323120. Epub 2023 Aug 21.
The generation of appropriate behavioral responses involves dedicated neuronal circuits. The cortico-striatal-thalamo-cortical loop is especially important for the expression of motor routines and habits. Defects in this circuitry are closely linked to obsessive stereotypic behaviors, hallmarks of neuropsychiatric diseases including autism spectrum disorders (ASDs) and obsessive-compulsive disorders (OCDs). However, our knowledge of the essential synaptic machinery required to maintain balanced neurotransmission and plasticity within the cortico-striatal circuitry remains fragmentary. Mutations in the large synaptic scaffold protein intersectin1 (ITSN1) have been identified in patients presenting with ASD symptoms including stereotypic behaviors, although a causal relationship between stereotypic behavior and intersectin function has not been established. We report here that deletion of the two closely related proteins ITSN1 and ITSN2 leads to severe ASD/OCD-like behavioral alterations and defective cortico-striatal neurotransmission in knockout (KO) mice. Cortico-striatal function was compromised at multiple levels in ITSN1/2-depleted animals. Morphological analyses showed that the striatum of intersectin KO mice is decreased in size. Striatal neurons exhibit reduced complexity and an underdeveloped dendritic spine architecture. These morphological abnormalities correlate with defects in cortico-striatal neurotransmission and plasticity as well as reduced N-methyl-D-aspartate (NMDA) receptor currents as a consequence of postsynaptic NMDA receptor depletion. Our findings unravel a physiological role of intersectin in cortico-striatal neurotransmission to counteract ASD/OCD. Moreover, we delineate a molecular pathomechanism for the neuropsychiatric symptoms of patients carrying intersectin mutations that correlates with the observation that NMDA receptor dysfunction is a recurrent feature in the development of ASD/OCD-like symptoms.
生成适当的行为反应涉及专门的神经元回路。皮质-纹状体-丘脑-皮质回路对于运动常规和习惯的表达尤为重要。该电路的缺陷与强迫性刻板行为密切相关,这些行为是神经精神疾病的标志,包括自闭症谱系障碍(ASD)和强迫症(OCD)。然而,我们对于维持皮质-纹状体电路中平衡的神经递质传递和可塑性所需的基本突触机制的了解仍然很零碎。在表现出 ASD 症状(包括刻板行为)的患者中,已经鉴定出大突触支架蛋白 intersectin1(ITSN1)的突变,尽管刻板行为和 intersectin 功能之间的因果关系尚未建立。我们在这里报告,删除两个密切相关的蛋白 ITSN1 和 ITSN2 会导致 knockout(KO)小鼠出现严重的 ASD/OCD 样行为改变和皮质-纹状体神经传递缺陷。ITSN1/2 耗尽的动物的皮质-纹状体功能在多个层面受到损害。形态分析表明,intersectin KO 小鼠的纹状体体积减小。纹状体神经元表现出复杂性降低和发育不良的树突棘结构。这些形态异常与皮质-纹状体神经传递和可塑性缺陷以及由于突触后 NMDA 受体耗竭导致的 N-甲基-D-天冬氨酸(NMDA)受体电流减少相关。我们的发现揭示了 intersectin 在皮质-纹状体神经传递中的生理作用,以对抗 ASD/OCD。此外,我们描绘了携带 intersectin 突变的患者的神经精神症状的分子发病机制,这与 NMDA 受体功能障碍是 ASD/OCD 样症状发展的反复特征的观察结果相关。