1] Department of Biology, The Johns Hopkins University, Baltimore, Maryland, USA. [2] Receptor Biology Section, National Institute of Neurological Disorders and Stroke (NINDS), National Institutes of Health (NIH), Bethesda, Maryland, USA.
Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, California, USA.
Nat Neurosci. 2014 Jan;17(1):56-64. doi: 10.1038/nn.3601. Epub 2013 Dec 15.
Neuroligins are postsynaptic cell adhesion molecules that are important for synaptic function through their trans-synaptic interaction with neurexins (NRXNs). The localization and synaptic effects of neuroligin-1 (NL-1, also called NLGN1) are specific to excitatory synapses with the capacity to enhance excitatory synapses dependent on synaptic activity or Ca(2+)/calmodulin kinase II (CaMKII). Here we report that CaMKII robustly phosphorylates the intracellular domain of NL-1. We show that T739 is the dominant CaMKII site on NL-1 and is phosphorylated in response to synaptic activity in cultured rodent neurons and sensory experience in vivo. Furthermore, a phosphodeficient mutant (NL-1 T739A) reduces the basal and activity-driven surface expression of NL-1, leading to a reduction in neuroligin-mediated excitatory synaptic potentiation. To the best of our knowledge, our results are the first to demonstrate a direct functional interaction between CaMKII and NL-1, two primary components of excitatory synapses.
神经黏附素是突触后细胞黏附分子,通过与神经连接蛋白(NRXNs)的跨突触相互作用,对突触功能至关重要。神经黏附素-1(NL-1,也称为 NLGN1)的定位和突触效应是兴奋性突触特有的,能够增强依赖于突触活动或 Ca(2+)/钙调蛋白激酶 II(CaMKII)的兴奋性突触。在这里,我们报告 CaMKII 能够强烈磷酸化 NL-1 的细胞内结构域。我们表明 T739 是 NL-1 上的主要 CaMKII 位点,并且在培养的啮齿动物神经元中的突触活动和体内感觉体验的刺激下发生磷酸化。此外,磷酸化缺陷突变体(NL-1 T739A)降低了 NL-1 的基础和活性驱动的表面表达,导致神经黏附素介导的兴奋性突触增强减少。据我们所知,我们的结果首次证明了 CaMKII 和 NL-1 之间的直接功能相互作用,这两者是兴奋性突触的两个主要组成部分。