Peking University Sixth Hospital, Peking University Institute of Mental Health, NHC Key Laboratory of Mental Health (Peking University), National Clinical Research Center for Mental Disorders (Peking University Sixth Hospital), Beijing 100191, China; National Clinical Research Center for Mental Disorders & Beijing Key Laboratory of Mental Disorders, Beijing Anding Hospital, Capital Medical University, Beijing 100088, China.
Shanghai Key Laboratory of Clinical Geriatric Medicine, Department of Cardiology, Huadong Hospital Affiliated to Fudan University, Shanghai 200040, China.
Cell Rep. 2019 Oct 1;29(1):49-61.e7. doi: 10.1016/j.celrep.2019.08.091.
Previous genetic and biological evidence converge on the involvement of synaptic dysfunction in schizophrenia, and OPCML, encoding a synaptic membrane protein, is reported to be genetically associated with schizophrenia. However, its role in the pathophysiology of schizophrenia remains largely unknown. Here, we found that Opcml is strongly expressed in the mouse hippocampus; ablation of Opcml leads to reduced phosphorylated cofilin and dysregulated F-actin dynamics, which disturbs the spine maturation. Furthermore, Opcml interacts with EphB2 to control the stability of spines by regulating the ephrin-EphB2-cofilin signaling pathway. Opcml-deficient mice display impaired cognitive behaviors and abnormal sensorimotor gating, which are similar to features in neuropsychiatric disorders such as schizophrenia. Notably, the administration of aripiprazole partially restores the abnormal behaviors in Opcml mice by increasing the phosphorylated cofilin level and facilitating spine maturation. We demonstrated a critical role of the schizophrenia-susceptible gene OPCML in spine maturation and cognitive behaviors via regulating the ephrin-EphB2-cofilin signaling pathway, providing further insights into the characteristics of schizophrenia.
先前的遗传和生物学证据表明,突触功能障碍与精神分裂症有关,而编码突触膜蛋白的 OPCML 也被报道与精神分裂症存在遗传关联。然而,其在精神分裂症病理生理学中的作用仍知之甚少。在这里,我们发现 Opcml 在小鼠海马体中强烈表达;Opcml 的缺失导致磷酸化的丝切蛋白减少和 F-肌动蛋白动力学失调,从而扰乱了棘突成熟。此外,Opcml 与 EphB2 相互作用,通过调节 ephrin-EphB2-丝切蛋白信号通路来控制棘突的稳定性。Opcml 缺失小鼠表现出认知行为障碍和异常的感觉运动门控,这与精神分裂症等神经精神障碍的特征相似。值得注意的是,阿立哌唑的给药通过增加磷酸化丝切蛋白水平和促进棘突成熟,部分恢复了 Opcml 小鼠的异常行为。我们通过调节 ephrin-EphB2-丝切蛋白信号通路,证明了精神分裂症易感基因 OPCML 在棘突成熟和认知行为中的关键作用,为精神分裂症的特征提供了进一步的见解。