Center for Metabolic Disease Research, Temple University Lewis Katz School of Medicine, Philadelphia, Pennsylvania; MD/PhD and Biomedical Sciences Graduate Program, Temple University Lewis Katz School of Medicine, Philadelphia, Pennsylvania.
Center for Metabolic Disease Research, Temple University Lewis Katz School of Medicine, Philadelphia, Pennsylvania; Department of Pathology and Laboratory Medicine, Temple University Lewis Katz School of Medicine, Philadelphia, Pennsylvania; Department of Molecular and Cellular Pharmacology, Peking University School of Pharmaceutical Sciences, Beijing, China.
Transl Res. 2020 Oct;224:55-70. doi: 10.1016/j.trsl.2020.05.001. Epub 2020 May 17.
NFκB signaling and protein trafficking network play important roles in various biological and pathological processes. NIK-and-IKK2-binding protein (NIBP), also known as trafficking protein particle complex 9 (TRAPPC9), is a prototype member of a novel protein family, and has been shown to regulate both NFκB signaling pathway and protein transport/trafficking. NIBP is extensively expressed in the nervous system and plays an important role in regulating neurogenesis and neuronal differentiation. NIBP/TRAPPC9 mutations have been linked to an autosomal recessive intellectual disability syndrome, called NIBP Syndrome, which is characterized by nonsyndromic autosomal recessive intellectual disability along with other symptoms such as obesity, microcephaly, and facial dysmorphia. As more cases of NIBP Syndrome are identified, new light is being shed on the role of NIBP/TRAPPC9 in the central nervous system developments and diseases. NIBP is also involved in the enteric nervous system. This review will highlight the importance of NIBP/TRAPPC9 in central and enteric nervous system diseases, and the established possible mechanisms for developing a potential therapeutic.
NFκB 信号转导和蛋白质运输网络在各种生物学和病理学过程中发挥着重要作用。NIK 和 IKK2 结合蛋白(NIBP),也称为运输蛋白颗粒复合物 9(TRAPPC9),是一个新型蛋白质家族的原型成员,已被证明可调节 NFκB 信号通路和蛋白质运输/运输。NIBP 在神经系统中广泛表达,在调节神经发生和神经元分化方面发挥着重要作用。NIBP/TRAPPC9 突变与常染色体隐性智力障碍综合征有关,称为 NIBP 综合征,其特征为常染色体隐性智力障碍,同时还伴有肥胖、小头畸形和面部畸形等其他症状。随着越来越多的 NIBP 综合征病例被发现,NIBP/TRAPPC9 在中枢神经系统发育和疾病中的作用也逐渐明朗。NIBP 还参与肠神经系统。本综述将重点介绍 NIBP/TRAPPC9 在中枢和肠神经系统疾病中的重要性,以及为开发潜在治疗方法而建立的可能机制。