Hu Ling, Chen Yi, Yang Cui-Ping, Huang Ying, Song Ning-Ning, Chen Jia-Yin, Sun Yu-Ling, Ding Yu-Qiang, Lang Bing
State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, Shanghai, China.
Key Laboratory of Arrhythmias, Ministry of Education, East Hospital, and Department of Anatomy and Neurobiology, Tongji University School of Medicine, Shanghai, China.
Front Cell Dev Biol. 2021 Jun 21;9:645368. doi: 10.3389/fcell.2021.645368. eCollection 2021.
Schizophrenia (SCZ) is a chronic and severe mental disease that affects around 1% of the population. The precise etiology of SCZ still remains largely unknown, and no conclusive mechanisms are firmly established. Recent advances in epidemiological and clinical investigation support an overwhelmingly strong neurodevelopmental origin for SCZ. Here, we demonstrated that Unc-51-like kinase 4 (Ulk4), a novel risk factor for major mental disorders including schizophrenia, is involved in the corticogenesis. Deletion of Ulk4 in mice led to significantly thinner layers of II-III, and V in the cerebral cortex, which was confirmed in conditional Ulk4 deletion mice achieved by Cre-loxp strategy. This abnormality might be caused by decreased intermediate neural progenitors and increased apoptosis. Thus, our data suggest that Ulk4 manipulates the behaviors of neural progenitors during brain development and, when functionally defective, leads to the reduction of specific cortical layers. This anomaly may increase predisposition to a range of neurodevelopmental disorders, including SCZ.
精神分裂症(SCZ)是一种慢性严重精神疾病,影响着约1%的人口。SCZ的确切病因在很大程度上仍然未知,尚未确立确凿的发病机制。流行病学和临床研究的最新进展有力支持了SCZ具有极强的神经发育起源。在此,我们证明了Unc-51样激酶4(Ulk4),一种包括精神分裂症在内的主要精神障碍的新型风险因素,参与了皮质发生过程。小鼠中Ulk4的缺失导致大脑皮层II-III层和V层显著变薄,这在通过Cre-loxp策略构建的条件性Ulk4缺失小鼠中得到证实。这种异常可能是由中间神经祖细胞减少和细胞凋亡增加所致。因此,我们的数据表明,Ulk4在大脑发育过程中调控神经祖细胞的行为,当其功能缺陷时,会导致特定皮质层减少。这种异常可能会增加包括SCZ在内的一系列神经发育障碍的易感性。