García-Cerro Susana, Gómez-Garrido Ana, Garcia Gonçalo, Crespo-Facorro Benedicto, Brites Dora
Translational Psychiatry Group, Ibis-Biomedicine Institute of Sevilla-CSIC, Manuel Siurot AV, 41013 Seville, Spain.
Spanish Network for Research in Mental Health (CIBERSAM), Monforte de Lemos AV, 3-5, 28029 Madrid, Spain.
Int J Mol Sci. 2024 Feb 28;25(5):2786. doi: 10.3390/ijms25052786.
MicroRNAs (miRNAs) play a crucial role in the regulation of gene expression levels and have been implicated in the pathogenesis of autism spectrum disorder (ASD) and schizophrenia (SCZ). In this study, we examined the adult expression profiles of specific miRNAs in the prefrontal cortex (PFC) of a neurodevelopmental mouse model for ASD and SCZ that mimics perinatal pathology, such as NMDA receptor hypofunction, and exhibits behavioral and neurophysiological phenotypes related to these disorders during adulthood. To model the early neuropathogenesis of the disorders, mouse pups were administered subcutaneously with ketamine (30 mg/Kg) at postnatal days 7, 9, and 11. We focused on a set of miRNAs most frequently altered in ASD (miR-451a and miR-486-3p) and in SCZ (miR-132-3p and miR-137-3p) according to human studies. Additionally, we explored miRNAs whose alterations have been identified in both disorders (miR-21-5p, miR-92a-2-5p, miR-144-3p, and miR-146a-5p). We placed particular emphasis on studying the sexual dimorphism in the dynamics of these miRNAs. Our findings revealed significant alterations in the PFC of this ASD- and SCZ-like mouse model. Specifically, we observed upregulated miR-451a and downregulated miR-137-3p. Furthermore, we identified sexual dimorphism in the expression of miR-132-3p, miR-137-3p, and miR-92a-2-5p. From a translational perspective, our results emphasize the potential involvement of miR-92a-2-5p, miR-132-3p, miR-137-3p, and miR-451a in the pathophysiology of ASD and SCZ and strengthen their potential as biomarkers and therapeutic targets of such disorders.
微小RNA(miRNA)在基因表达水平的调控中发挥着关键作用,并与自闭症谱系障碍(ASD)和精神分裂症(SCZ)的发病机制有关。在本研究中,我们检测了一种模仿围产期病理(如NMDA受体功能低下)的ASD和SCZ神经发育小鼠模型成年期前额叶皮质(PFC)中特定miRNA的表达谱,该模型在成年期表现出与这些疾病相关的行为和神经生理表型。为了模拟这些疾病的早期神经发病机制,在出生后第7、9和11天给幼鼠皮下注射氯胺酮(30 mg/Kg)。根据人类研究,我们重点关注了一组在ASD(miR-451a和miR-486-3p)和SCZ(miR-132-3p和miR-137-3p)中最常发生改变的miRNA。此外,我们还探索了在这两种疾病中均已发现其改变的miRNA(miR-21-5p、miR-92a-2-5p、miR-144-3p和miR-146a-5p)。我们特别强调研究这些miRNA动态变化中的性别差异。我们的研究结果揭示了这种ASD和SCZ样小鼠模型的PFC中存在显著改变。具体而言,我们观察到miR-451a上调,miR-137-3p下调。此外,我们还发现了miR-132-3p、miR-137-3p和miR-92a-2-5p表达中的性别差异。从转化医学的角度来看,我们的结果强调了miR-92a-2-5p、miR-132-3p、miR-137-3p和miR-451a可能参与了ASD和SCZ的病理生理学过程,并增强了它们作为这些疾病生物标志物和治疗靶点的潜力。