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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Carboxypeptidase E cytoplasmic tail mediates localization of synaptic vesicles to the pre-active zone in hypothalamic pre-synaptic terminals.
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Carboxypeptidase E cytoplasmic tail mediates localization of synaptic vesicles to the pre-active zone in hypothalamic pre-synaptic terminals.

机译:羧肽酶E的细胞质尾部介导突触小泡在下丘脑突触前末端的主动区。

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摘要

How synaptic vesicles (SVs) are localized to the pre-active zone (5-200 nm beneath the active zone) in the nerve terminal, which may represent the slow response SV pool, is not fully understood. Electron microscopy revealed the number of SVs located in the pre-active zone, was significantly decreased in hypothalamic neurons of carboxypeptidase E knockout (CPE-KO) mice compared with wild-type mice. Additionally, we found K(+)-stimulated glutamate secretion from hypothalamic embryonic neurons was impaired in CPE-KO mice. Biochemical studies indicate that SVs from the hypothalamus of wild-type mice and synaptic-like microvesicles from PC12 cells contain a transmembrane form of CPE, with a cytoplasmic tail (CPE(C10)), maybe involved in synaptic function. Yeast two-hybrid and pull-down experiments showed that the CPE cytoplasmic tail interacted with gamma-adducin, which binds actin enriched at the nerve terminal. Total internal reflective fluorescence (TIRF) microscopy using PC12 cells as a model showed that expression of GFP-CPE(C15) reduced the steady-state level of synaptophysin-mRFP containing synaptic-like microvesicles accumulated in the area within 200 nm from the sub-plasma membrane (TIRF zone). Our findings identify the CPE cytoplasmic tail, as a new mediator for the localization of SVs in the actin-rich pre-active zone in hypothalamic neurons and the TIRF zone of PC12 cells.
机译:尚未完全了解突触小泡(SVs)如何定位到神经末梢的活动前区(活动区下方5-200 nm),这可能代表了反应迟钝的SV池。电镜观察发现,与野生型小鼠相比,羧肽酶E敲除(CPE-KO)小鼠的下丘脑神经元中位于前活跃区的SV数量明显减少。此外,我们发现在CPE-KO小鼠中,下丘脑胚胎神经元的K(+)刺激的谷氨酸分泌受到损害。生化研究表明,来自野生型小鼠下丘脑的SVs和来自PC12细胞的突触样微泡包含跨膜形式的CPE,其胞质尾巴(CPE(C10))可能参与突触功能。酵母两杂交和下拉实验表明,CPE胞质尾巴与γ-adducin相互作用,后者与富含神经末梢的肌动蛋白结合。使用PC12细胞作为模型的全内反射荧光(TIRF)显微镜显示,GFP-CPE(C15)的表达降低了突触素-mRFP的稳态水平,该突触素-mRFP包含在距亚核200 nm以内的区域内积累的突触样微囊泡。质膜(TIRF区)。我们的发现确定CPE胞质尾巴是下丘脑神经元富含肌动蛋白的活性区和PC12细胞TIRF区中SVs定位的新介体。

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