Noh Kyungchul, Park Jung-Cheol, Han Jung-Soo, Lee Sung Joong
Department of Physiology and Neuroscience, Dental Research Institute, Seoul National University School of Dentistry, Seoul 08826, Korea.
Department of Biological Science, Konkuk University, Seoul 05029, Korea.
Exp Neurobiol. 2020 Feb 29;29(1):1-10. doi: 10.5607/en.2020.29.1.1.
Cell-to-cell adhesion is important for maintenance of brain structure and function. Abnormal neuronal cell adhesion and loss of its connectivity are considered a main cause of psychiatric disorders such as major depressive disorder (MDD). Various cell adhesion molecules (CAMs) are involved in neuronal cell adhesions and thereby affect brain functions such as learning and memory, cognitive functions, and psychiatric functions. Compared with other CAMs, neuronal growth regulator 1 (Negr1) has a distinct functioning mechanism in terms of its cross-talk with cytokine receptor signaling. Negr1 is a member of the immunoglobulin LON (IgLON) family of proteins and is involved in neuronal outgrowth, dendritic arborization, and synapse formation. In humans, Negr1 is a risk gene for obesity based on a genome-wide association study. More recently, accumulating evidence supports that it also plays a critical role in psychiatric disorders. In this review, we discuss the recent findings on the role of Negr1 in MDD, focusing on its regulatory mechanism. We also provide evidence of putative involvement of Negr1 in other psychiatric disorders based on the novel behavioral phenotypes of Negr1 knockout mice.
细胞间黏附对于维持大脑结构和功能很重要。异常的神经元细胞黏附及其连接性丧失被认为是诸如重度抑郁症(MDD)等精神疾病的主要原因。多种细胞黏附分子(CAMs)参与神经元细胞黏附,从而影响大脑功能,如学习和记忆、认知功能以及精神功能。与其他CAMs相比,神经元生长调节因子1(Negr1)在与细胞因子受体信号的相互作用方面具有独特的作用机制。Negr1是免疫球蛋白LON(IgLON)蛋白家族的成员,参与神经元生长、树突分支和突触形成。在人类中,基于全基因组关联研究,Negr1是肥胖的风险基因。最近,越来越多的证据支持它在精神疾病中也起着关键作用。在这篇综述中,我们讨论了Negr1在MDD中作用的最新发现,重点关注其调节机制。我们还基于Negr1基因敲除小鼠的新行为表型,提供了Negr1可能参与其他精神疾病的证据。