Pizzo R, Lamarca A, Sassoè-Pognetto M, Giustetto M
Department of Neuroscience, University of Turin, Corso Massimo D'Azeglio 52, 10126 Turin, Italy.
Department of Neuroscience, University of Turin, Corso Massimo D'Azeglio 52, 10126 Turin, Italy; National Institute of Neuroscience-Italy, Corso Massimo D'Azeglio 52, 10126 Turin, Italy.
Neuroscience. 2020 Oct 1;445:130-143. doi: 10.1016/j.neuroscience.2019.08.033. Epub 2019 Aug 28.
Mutations in the CDKL5 (cyclin-dependent kinase-like 5) gene cause CDKL5 Deficiency Disorder (CDD), a severe neurodevelopmental syndrome where patients exhibit early-onset seizures, intellectual disability, stereotypies, limited or absent speech, autism-like symptoms and sensory impairments. Mounting evidences indicate that disrupted sensory perception and processing represent core signs also in mouse models of CDD; however we have very limited knowledge on their underlying causes. In this study, we investigated how CDKL5 deficiency affects synaptic organization and experience-dependent plasticity in the thalamo-cortical (TC) pathway carrying whisker-related tactile information to the barrel cortex (BC). By using synapse-specific antibodies and confocal microscopy, we found that Cdkl5-KO mice display a lower density of TC synapses in the BC that was paralleled by a reduction of cortico-cortical (CC) connections compared to wild-type mice. These synaptic defects were accompanied by reduced BC activation, as shown by a robust decrease of c-fos immunostaining, and atypical behavioral responses to whisker-mediated tactile stimulation. Notably, a 2-day paradigm of enriched whisker stimulation rescued both number and configuration of excitatory synapses in Cdkl5-KO mice, restored cortical activity and normalized behavioral responses to wild-type mice levels. Our findings disclose a novel and unsuspected role of CDKL5 in controlling the organization and experience-induced modifications of excitatory connections in the BC and indicate how mutations of CDKL5 produce failures in higher-order processing of somatosensory stimuli. This article is part of a Special Issue entitled: Animal Models of Neurodevelopmental Disorders.
细胞周期蛋白依赖性激酶样5(CDKL5)基因的突变会导致CDKL5缺陷障碍(CDD),这是一种严重的神经发育综合征,患者会出现早发性癫痫、智力残疾、刻板动作、言语受限或缺失、自闭症样症状以及感觉障碍。越来越多的证据表明,感觉感知和处理功能紊乱也是CDD小鼠模型的核心症状;然而,我们对其潜在原因的了解非常有限。在这项研究中,我们调查了CDKL5缺陷如何影响携带与胡须相关触觉信息至桶状皮层(BC)的丘脑-皮层(TC)通路中的突触组织和经验依赖性可塑性。通过使用突触特异性抗体和共聚焦显微镜,我们发现与野生型小鼠相比,Cdkl5基因敲除(KO)小鼠的BC中TC突触密度较低,同时皮质-皮质(CC)连接减少。这些突触缺陷伴随着BC激活的减少,如c-fos免疫染色的显著降低所示,以及对胡须介导的触觉刺激的非典型行为反应。值得注意 的是,为期2天的丰富胡须刺激范式挽救了Cdkl5-KO小鼠中兴奋性突触的数量和结构,恢复了皮质活动,并使行为反应恢复到野生型小鼠水平。我们的研究结果揭示了CDKL5在控制BC中兴奋性连接的组织和经验诱导的修饰方面的一个新的、意想不到的作用,并表明CDKL5突变如何导致体感刺激的高阶处理失败。本文是名为:神经发育障碍动物模型的特刊的一部分。