Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Brain and Mind Research Center, Nagoya University, Nagoya, Aichi, Japan.
Transl Psychiatry. 2024 May 28;14(1):216. doi: 10.1038/s41398-024-02952-6.
Genetic factors significantly affect the pathogenesis of psychiatric disorders. However, the specific pathogenic mechanisms underlying these effects are not fully understood. Recent extensive genomic studies have implicated the protocadherin-related 15 (PCDH15) gene in the onset of psychiatric disorders, such as bipolar disorder (BD). To further investigate the pathogenesis of these psychiatric disorders, we developed a mouse model lacking Pcdh15. Notably, although PCDH15 is primarily identified as the causative gene of Usher syndrome, which presents with visual and auditory impairments, our mice with Pcdh15 homozygous deletion (Pcdh15-null) did not exhibit observable structural abnormalities in either the retina or the inner ear. The Pcdh15-null mice showed very high levels of spontaneous motor activity which was too disturbed to perform standard behavioral testing. However, the Pcdh15 heterozygous deletion mice (Pcdh15-het) exhibited enhanced spontaneous locomotor activity, reduced prepulse inhibition, and diminished cliff avoidance behavior. These observations agreed with the symptoms observed in patients with various psychiatric disorders and several mouse models of psychiatric diseases. Specifically, the hyperactivity may mirror the manic episodes in BD. To obtain a more physiological, long-term quantification of the hyperactive phenotype, we implanted nano tag® sensor chips in the animals, to enable the continuous monitoring of both activity and body temperature. During the light-off period, Pcdh15-null exhibited elevated activity and body temperature compared with wild-type (WT) mice. However, we observed a decreased body temperature during the light-on period. Comprehensive brain activity was visualized using c-Fos mapping, which was assessed during the activity and temperature peak and trough. There was a stark contrast between the distribution of c-Fos expression in Pcdh15-null and WT brains during both the light-on and light-off periods. These results provide valuable insights into the neural basis of the behavioral and thermal characteristics of Pcdh15-deletion mice. Therefore, Pcdh15-deletion mice can be a novel model for BD with mania and other psychiatric disorders, with a strong genetic component that satisfies both construct and surface validity.
遗传因素对精神疾病的发病机制有显著影响。然而,这些影响的具体发病机制尚不完全清楚。最近广泛的基因组研究表明原钙黏蛋白 15(PCDH15)基因与精神疾病的发病有关,如双相情感障碍(BD)。为了进一步研究这些精神疾病的发病机制,我们开发了一种缺乏 Pcdh15 的小鼠模型。值得注意的是,虽然 PCDH15 主要被确定为导致伴有视觉和听觉障碍的 Usher 综合征的致病基因,但我们的 Pcdh15 纯合缺失(Pcdh15-null)小鼠的视网膜或内耳均未表现出明显的结构异常。Pcdh15-null 小鼠表现出非常高的自发运动活性,其活动过于紊乱,无法进行标准行为测试。然而,Pcdh15 杂合缺失(Pcdh15-het)小鼠表现出增强的自发运动活性、降低的前脉冲抑制和减少的悬崖回避行为。这些观察结果与各种精神疾病患者和几种精神疾病的小鼠模型观察到的症状一致。具体而言,过度活跃可能反映了 BD 中的躁狂发作。为了更生理、长期地量化过度活跃的表型,我们在动物体内植入了纳米标签®传感器芯片,以实现对活动和体温的连续监测。在熄灯期间,与野生型(WT)小鼠相比,Pcdh15-null 表现出更高的活动和体温。然而,我们观察到在光照期间体温下降。使用 c-Fos 映射对综合大脑活动进行可视化,在活动和温度高峰和低谷期间进行评估。在光照和熄灯期间,Pcdh15-null 和 WT 大脑中 c-Fos 表达的分布存在鲜明对比。这些结果为 Pcdh15 缺失小鼠的行为和体温特征的神经基础提供了有价值的见解。因此,Pcdh15 缺失小鼠可以成为具有躁狂和其他精神疾病的 BD 的新型模型,具有强烈的遗传成分,同时满足结构和表面有效性。