Owczarek Sylwia, Bang Marie Louise, Berezin Vladimir
Laboratory of Neural Plasticity, Department of Neuroscience and Pharmacology, University of Copenhagen, 2200 Copenhagen, Denmark ; Research Laboratory for Stereology and Neuroscience, Bispebjerg Hospital, 2400 Copenhagen, Denmark.
Laboratory of Neural Plasticity, Department of Neuroscience and Pharmacology, University of Copenhagen, 2200 Copenhagen, Denmark.
Neural Plast. 2015;2015:167308. doi: 10.1155/2015/167308. Epub 2015 May 20.
Neurexins (NXs) and neuroligins (NLs) are cell adhesion molecules that are localized at opposite sites of synaptic membranes. They interact with each other to promote the assembly, maintenance, and function of synapses in the central nervous system. Both NX and NL are cleaved from a membrane-attached intracellular domain in an activity-dependent manner, generating the soluble ectodomain of NX or NL. Expression of the NX1 and NX3 genes in the brain appears to be regulated by a schizophrenia-related protein, DISC1. Here, we show that soluble ecto-NX1β can regulate the expression of DISC1 and induce signaling downstream of DISC1. We also show that NL1 binds to a well-characterized DISC1 interaction partner, Kal-7, and this interaction can be compromised by DISC1. Our results indicate that the NX/NL synaptic complex is intrinsically involved in the regulation of DISC1 function, thus contributing to a better understanding of the pathology of schizophrenia.
神经连接蛋白(NXs)和神经配体(NLs)是细胞粘附分子,定位于突触膜的相对位点。它们相互作用以促进中枢神经系统中突触的组装、维持和功能。NX和NL都以活性依赖的方式从膜附着的细胞内结构域裂解,产生NX或NL的可溶性胞外结构域。大脑中NX1和NX3基因的表达似乎受一种与精神分裂症相关的蛋白质DISC1调控。在此,我们表明可溶性胞外NX1β可调控DISC1的表达并诱导DISC1下游的信号传导。我们还表明NL1与一个已明确的DISC1相互作用伴侣Kal-7结合,且这种相互作用会被DISC1破坏。我们的结果表明,NX/NL突触复合体本质上参与DISC1功能的调控,从而有助于更好地理解精神分裂症的病理学。