Pan Miao, Liu Pin-Wu, Ozawa Yukihiro, Arima-Yoshida Fumiko, Dong Geyao, Sawahata Masahito, Mori Daisuke, Nagase Masashi, Fujii Hajime, Ueda Shuhei, Yabuuchi Yurie, Liu Xinzi, Narita Hajime, Konno Ayumu, Hirai Hirokazu, Ozaki Norio, Yamada Kiyofumi, Kidokoro Hiroyuki, Bito Haruhiko, Mizoguchi Hiroyuki, M Watabe Ayako, Horigane Shin-Ichiro, Takemoto-Kimura Sayaka
Department of Neuroscience, Research Institute of Environmental Medicine, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, Aichi, Japan.
Molecular/Cellular Neuroscience, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, Japan.
Transl Psychiatry. 2025 Mar 26;15(1):95. doi: 10.1038/s41398-025-03316-4.
Intellectual disability (ID) is a neurodevelopmental disorder (NDD) characterized by impairments in intellectual and adaptive functioning, and is highly co-morbid with other NDDs. Recently, de novo missense variants in the gene, CAMK2A, which encodes calcium/calmodulin-dependent protein kinase IIα (CaMKIIα), an abundant neuronal protein crucial for synaptic plasticity, learning and memory, have been implicated in ID. However, the causative impact of these mutations remains underexplored. In this study, we developed a heterozygous knock-in mouse model carrying the most prevalent ID-associated CAMK2A de novo missense variant, P212L, as a gain-of-function allele. The knock-in mice exhibited increased autophosphorylation of CaMKIIα, indicative of exuberant kinase activity, and consistently showed dendritic spine abnormalities and exaggerated hippocampal long-term potentiation induced by a subthreshold low-frequency stimulation. Furthermore, a comprehensive behavioral evaluation, including learning and memory tasks, revealed prominent phenotypes recapitulating the complex clinical phenotypes of humans with ID/NDDs harboring the same variant. Taken together, we propose that aberrant enhancement of CaMKIIα signaling by the heterozygous P212L mutation underlies a subset of ID/NDD features. These findings provide new insights into the pathogenesis of ID/NDDs, specifically through the genetic up-shifting of the critical memory regulator, CaMKII. Additionally, the established mouse model, with both construct and face validity, is expected to significantly contribute to the understanding and future therapeutic development of ID/NDDs.
智力残疾(ID)是一种神经发育障碍(NDD),其特征是智力和适应性功能受损,并且与其他NDD高度共病。最近,编码钙/钙调蛋白依赖性蛋白激酶IIα(CaMKIIα)的基因CAMK2A中的新生错义变体与ID有关,CaMKIIα是一种丰富的神经元蛋白,对突触可塑性、学习和记忆至关重要。然而,这些突变的致病影响仍未得到充分探索。在本研究中,我们构建了一个杂合敲入小鼠模型,携带最常见的与ID相关的CAMK2A新生错义变体P212L,作为功能获得性等位基因。敲入小鼠表现出CaMKIIα的自磷酸化增加,表明激酶活性旺盛,并始终表现出树突棘异常以及阈下低频刺激诱导的海马长时程增强反应过度。此外,包括学习和记忆任务在内的全面行为评估揭示了突出的表型,重现了携带相同变体的ID/NDD患者的复杂临床表型。综上所述,我们认为杂合P212L突变导致的CaMKIIα信号异常增强是ID/NDD部分特征的基础。这些发现为ID/NDD的发病机制提供了新的见解,特别是通过关键记忆调节因子CaMKII的基因上调。此外,所建立的具有结构效度和表面效度的小鼠模型有望对ID/NDD的理解和未来治疗发展做出重大贡献。