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Analysis of Synaptotagmin SV2 and Rab3 Expression in Cortical Glutamatergic and GABAergic Axon Terminals

机译:皮质谷氨酸和GABA能轴突末端中突触标签素SV2和Rab3表达的分析。

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摘要

We investigated whether cortical glutamatergic and GABAergic release machineries can be differentiated on the basis of the nature and amount of proteins they express, by performing a quantitative analysis of the degree of co-localization of synaptotagmin (SYT) 1 and 2, synaptic vesicle protein 2 (SV2) A and B, and Rab3a and c in VGLUT1+, VGLUT2+, and VGAT+ terminals and synaptic vesicles (SVs) in rat cerebral cortex. Co-localization studies showed that VGLUT1 puncta had high levels of SV2A and B and of Rab3c, intermediate levels of SYT1, and low levels of SYT2 and Rab3c; VGLUT2 puncta exhibited intermediate levels of all presynaptic proteins studied; whereas vesicular GABA transporter (VGAT) puncta had high levels of SV2A and SYT2, intermediate levels of SYT1, Rab3a, and Rab3c, and low levels of SV2B. Since SV2B is reportedly expressed by glutamatergic neurons and we observed SV2B expression in VGAT puncta, we performed electron microscopic studies and found SV2B positive axon terminals forming symmetric synapses. Immunoisolation studies showed that the expression levels of the protein isoforms varied in the three populations of SVs. Expression of SYT1 was highest in VGLUT1–SVs, while SYT2 expression was similar in the three SV groups. Expression of SV2A was similarly high in all three SV populations, except for SV2B levels that were very low in VGAT SVs. Finally, Rab3a levels were similar in the three SV groups, while Rab3c levels were highest in VGLUT1–SVs. These quantitative results extend our previous studies on the differential expression of presynaptic proteins involved in neurotransmitter release in GABAergic and glutamatergic terminals and indicate that heterogeneity of the respective release machineries can be generated by the differential complement of SV proteins involved in distinct stages of the release process.
机译:我们通过对突触小蛋白(SYT)1和2,突触小泡蛋白2的共定位程度进行定量分析,研究了皮质谷氨酸和GABA能释放机制是否可以根据它们表达的蛋白质的性质和数量来区分。 (SV2)A和B,以及VGLUT1 +,VGLUT2 +和VGAT +末端以及大鼠大脑皮层的突触小泡(SVs)中的Rab3a和c。共定位研究表明,VGLUT1点具有较高水平的SV2A和B和Rab3c,中等水平的SYT1,以及较低水平的SYT2和Rab3c。 VGLUT2点点在所有研究的突触前蛋白中均表现出中等水平。而囊泡GABA转运蛋白(VGAT)点的SV2A和SYT2含量高,SYT1,Rab3a和Rab3c的含量中等,而SV2B的含量低。由于据报道SV2B由谷氨酸能神经元表达,并且我们在VGAT点中观察到SV2B的表达,因此我们进行了电子显微镜研究,发现SV2B阳性轴突末端形成了对称突触。免疫分离研究表明,在三个SV种群中,蛋白质同工型的表达水平有所不同。 SYT1的表达在VGLUT1-SVs中最高,而SYT2的表达在三个SV组中相似。除了在VGAT SV中非常低的SV2B水平外,在所有三个SV群体中SV2A的表达都类似地高。最后,三个SV组的Rab3a水平相似,而VGLUT1–SV中的Rab3c水平最高。这些定量结果扩展了我们先前对参与GABA能和谷氨酸能终末神经递质释放的突触前蛋白差异表达的研究,并表明各个释放机制的异质性可以由参与释放过程不同阶段的SV蛋白的差异补体产生。 。

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