Jiang Wei, Wei Mengping, Liu Mengna, Pan Yunlong, Cao Dong, Yang Xiaofei, Zhang Chen
Key Laboratory of Cognitive Science, Hubei Key Laboratory of Medical Information Analysis and Tumor Diagnosis and Treatment, Laboratory of Membrane Ion Channels and Medicine, College of Biomedical Engineering, South-Central University for Nationalities, Wuhan 430074, China.
State Key Laboratory of Membrane Biology, PKU-IDG/McGovern Institute for Brain Research, School of Life Sciences, Peking University, Beijing 100871, China, and.
J Neurosci. 2017 Oct 11;37(41):9828-9843. doi: 10.1523/JNEUROSCI.0729-17.2017. Epub 2017 Sep 4.
The proper formation of synapses-specialized unitary structures formed between two neurons-is critical to mediating information flow in the brain. Synaptic cell adhesion molecules (CAMs) are thought to participate in the initiation of the synapse formation process. However, functional analysis demonstrates that most well known synaptic CAMs regulate synaptic maturation and plasticity rather than synapse formation, suggesting that either CAMs work synergistically in the process of forming synapses or more CAMs remain to be found. By screening for unknown CAMs using a co-culture system, we revealed that protein tyrosine phosphatase receptor type O (PTPRO) is a potent CAM that induces the formation of artificial synapse clusters in co-cultures of human embryonic kidney 293 cells and hippocampal neurons cultured from newborn mice regardless of gender. PTPRO was enriched in the mouse brain and localized to postsynaptic sites at excitatory synapses. The overexpression of PTPRO in cultured hippocampal neurons increased the number of synapses and the frequency of miniature EPSCs (mEPSCs). The knock-down (KD) of PTPRO expression in cultured neurons by short hairpin RNA (shRNA) reduced the number of synapses and the frequencies of the mEPSCs. The effects of shRNA KD were rescued by expressing either full-length PTPRO or a truncated PTPRO lacking the cytoplasmic domain. Consistent with these results, the N-terminal extracellular domain of PTPRO was required for its synaptogenic activity in the co-culture assay. Our data show that PTPRO is a synaptic CAM that serves as a potent initiator of the formation of excitatory synapses. The formation of synapses is critical for the brain to execute its function and synaptic cell adhesion molecules (CAMs) play essential roles in initiating the formation of synapses. By screening for unknown CAMs using a co-culture system, we revealed that protein tyrosine phosphatase receptor type O (PTPRO) is a potent CAM that induces the formation of artificial synapse clusters. Using loss-of-function and gain-of-function approaches, we show that PTPRO promotes the formation of excitatory synapses. The N-terminal extracellular domain of PTPRO was required for its synaptogenic activity in cultured hippocampal neurons and the co-culture assay. Together, our data show that PTPRO is a synaptic CAM that serves as a potent initiator of synapse formation.
突触是两个神经元之间形成的特化单一结构,其正常形成对于介导大脑中的信息流至关重要。突触细胞粘附分子(CAMs)被认为参与突触形成过程的起始。然而,功能分析表明,大多数知名的突触CAMs调节突触成熟和可塑性而非突触形成,这表明CAMs要么在突触形成过程中协同作用,要么还有更多的CAMs有待发现。通过使用共培养系统筛选未知的CAMs,我们发现蛋白酪氨酸磷酸酶受体O型(PTPRO)是一种有效的CAM,它能在人胚胎肾293细胞与新生小鼠海马神经元的共培养物中诱导人工突触簇的形成,且与性别无关。PTPRO在小鼠脑中富集,并定位于兴奋性突触的突触后位点。在培养的海马神经元中过表达PTPRO增加了突触数量和微小兴奋性突触后电流(mEPSCs)的频率。通过短发夹RNA(shRNA)敲低培养神经元中PTPRO的表达减少了突触数量和mEPSCs的频率。通过表达全长PTPRO或缺乏胞质结构域的截短PTPRO可挽救shRNA敲低的效应。与这些结果一致,在共培养实验中,PTPRO的N端胞外结构域是其突触生成活性所必需的。我们的数据表明,PTPRO是一种突触CAM,可作为兴奋性突触形成的有效启动子。突触的形成对于大脑执行其功能至关重要,而突触细胞粘附分子(CAMs)在启动突触形成中起重要作用。通过使用共培养系统筛选未知的CAMs,我们发现蛋白酪氨酸磷酸酶受体O型(PTPRO)是一种能诱导人工突触簇形成的有效CAM。使用功能丧失和功能获得方法,我们表明PTPRO促进兴奋性突触的形成。在培养的海马神经元和共培养实验中,PTPRO的N端胞外结构域是其突触生成活性所必需的。总之,我们的数据表明,PTPRO是一种突触CAM,可作为突触形成的有效启动子。