认知科学重点实验室,湖北省医学信息分析与肿瘤诊疗重点实验室,膜离子通道与药物研发实验室, 中南民族大学生物医学工程学院,武汉 430074
国家自然科学基金(31670850)和中南民族大学基础研究基金(CZY19022和CZY19040)
Key Laboratory of Cognitive Science,Hubei Key Laboratory of Medical Information Analysis and Tumor Diagnosis & Treatment, Laboratory of Membrane Ion Channels and Medicine,College of Biomedical Engineering, South-Central University for Nationalities,Wuhan 430074,China
the National Science Foundation of China (31670850) and the Fundamental Research Funds for the Central Universities, South-Central University for Nationalities (CZY19022 and CZY19040)
Syntaxin-1是一种多结构域蛋白,通过与synaptobrevin-2和SNAP-25形成SNARE复合体调节囊泡融合。然而,syntaxin-1在突触形成过程中是否发挥作用,目前尚不清楚。我们的研究表明了syntaxin-1的表达水平与突触形成过程高度相关。Syntaxin-1的R151A和I155A突变影响其在突触形成中的促进作用,而Habc结构域或跨膜结构域在突触形成中无显著作用。我们的结果表明,syntaxin-1通过激活突触囊泡释放来加速突触的形成。
Syntaxin-1, known as a multi-domain protein, regulates vesicle fusion by forming SNARE complex with synaptobrevin-2 and SNAP-25. However, the role of syntaxin-1 in synapse formation remains uncovered. Here we demonstrated that the expression level of syntaxin-1 was highly associated with the process of synaptogenesis. The R151A and I155A mutations but not Habc or transmembrane domain truncations of syntaxin-1 impaired its facilitation in synapse formation. Our results suggested that syntaxin-1 accelerated synapse formation via activating synaptic vesicle release.
裴青,林寅,荣伊,刘孟雪,吴世平,阳小飞. Syntaxin-1通过激活突触递质传递加速早期突触的形成[J].生物化学与生物物理进展,2020,47(7):626-633
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