Mariga Abigail, Glaser Juliane, Mathias Leo, Xu Desheng, Xiao Meifang, Worley Paul, Ninan Ipe, Chao Moses V
Cell and Molecular Biology Program, New York University, Langone Medical Center, New York, NY 10016, USA; Department of Cell Biology, Skirball Institute of Bimolecular Medicine, NYU Langone Medical Center, New York, NY 10016, USA.
Unit of Genetics and Biology of Development, Institut Curie, 75005 Paris, France.
Cell Rep. 2015 Dec 1;13(9):1747-56. doi: 10.1016/j.celrep.2015.10.064. Epub 2015 Nov 19.
One of the cardinal features of neural development and adult plasticity is the contribution of activity-dependent signaling pathways. However, the interrelationships between different activity-dependent genes are not well understood. The immediate early gene neuronal-activity-regulated pentraxin (NPTX2 or Narp) encodes a protein that has been associated with excitatory synaptogenesis, AMPA receptor aggregation, and the onset of critical periods. Here, we show that Narp is a direct transcriptional target of brain-derived neurotrophic factor (BDNF), another highly regulated activity-dependent gene involved in synaptic plasticity. Unexpectedly, Narp is bidirectionally regulated by BDNF. Acute BDNF withdrawal results in downregulation of Narp, whereas transcription of Narp is greatly enhanced by BDNF. Furthermore, our results show that BDNF directly regulates Narp to mediate glutamatergic transmission and mossy fiber plasticity. Hence, Narp serves as a significant epistatic target of BDNF to regulate synaptic plasticity during periods of dynamic activity.
神经发育和成人可塑性的主要特征之一是依赖活动的信号通路的作用。然而,不同的依赖活动的基因之间的相互关系尚未得到很好的理解。即刻早期基因神经元活动调节五聚体蛋白(NPTX2或Narp)编码一种与兴奋性突触形成、AMPA受体聚集以及关键期的开始有关的蛋白质。在这里,我们表明Narp是脑源性神经营养因子(BDNF)的直接转录靶点,BDNF是另一个高度受调控的参与突触可塑性的依赖活动的基因。出乎意料的是,Narp受BDNF的双向调控。急性撤除BDNF会导致Narp下调,而BDNF会极大地增强Narp的转录。此外,我们的结果表明,BDNF直接调节Narp以介导谷氨酸能传递和苔藓纤维可塑性。因此,在动态活动期间,Narp作为BDNF的一个重要上位靶点来调节突触可塑性。