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首页> 外文期刊>Neuropathology and applied neurobiology >Expression pattern of synaptic vesicle protein 2 (SV2) isoforms in patients with temporal lobe epilepsy and hippocampal sclerosis
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Expression pattern of synaptic vesicle protein 2 (SV2) isoforms in patients with temporal lobe epilepsy and hippocampal sclerosis

机译:颞叶癫痫和海马硬化患者突触小泡蛋白2(SV2)亚型的表达模式

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Aims: Synaptic vesicle proteins 2 (SV2) are neuronal vesicles membrane glycoproteins that appear as important targets in the treatment of partial and generalized epilepsies. Therefore, we analysed the expression of SV2 isoforms in the hippocampus of patients with temporal lobe epilepsy (TLE). Methods: SV2A, SV2B and SV2C immunostaining and QuantiGene branched DNA assay were performed on biopsies from 31 consecutive TLE patients with mesial temporal sclerosis (MTS) and compared with 10 autopsy controls. SV2 expression was further compared with Timm's staining, and synaptophysin, Zinc transporter 3 (ZnT3), dynorphin, vesicular glutamate transporter 1 (VGLUT1) and vesicular GABA transporter (VGAT) expression. Results: In TLE patients, SV2A and SV2B expression was decreased in areas of synaptic loss. SV2C, which is weakly expressed or absent in the hippocampus of controls, was overexpressed in 10/11 cases with classical MTS1A and mossy fibre sprouting but not in cases with other types of MTS. SV2C staining was located in the inner molecular layer of the dentate gyrus and colocalized with dynorphin, ZnT3 and VGLUT1, suggesting selective expression in presynaptic glutamatergic Zn2+-rich terminals of abnormal sprouting fibres. SV2 expression patterns correlated with histological subtypes of MTS, but not with clinical features or therapeutic regimens in this patient cohort. Conclusion: In classical MTS1A, the expression of SV2 isoforms is altered with a marked decrease of SV2A and SV2B paralleling synaptic loss and a selective increase of SV2C in sprouting mossy fibres. These findings suggest a different physiology of sprouting synapses and the possibility to target them with SV2C-specific strategies.
机译:目的:突触小泡蛋白2(SV2)是神经元小泡膜糖蛋白,在部分和广泛性癫痫的治疗中作为重要的靶点而出现。因此,我们分析了颞叶癫痫(TLE)患者海马中SV2亚型的表达。方法:对31例连续性TLE患者的颞叶硬化症(MTS)的活检进行了SV2A,SV2B和SV2C免疫染色以及QuantiGene分支DNA检测,并与10例尸检对照进行了比较。进一步将SV2表达与Timm染色,突触素,锌转运蛋白3(ZnT3),强啡肽,谷氨酸囊泡转运蛋白1(VGLUT1)和囊泡GABA转运蛋白(VGAT)表达进行了比较。结果:在TLE患者中,在突触损失区域中SV2A和SV2B表达降低。 SV2C在对照海马中弱表达或不表达,在经典MTS1A和苔藓纤维发芽的10/11病例中过表达,而在其他类型的MTS情况下则不表达。 SV2C染色位于齿状回的内分子层中,并与强啡肽,ZnT3和VGLUT1共同定位,表明在异常发芽纤维的突触前谷氨酸能富Zn2 +末端中有选择性表达。 SV2表达模式与MTS的组织学亚型相关,但与该患者队列的临床特征或治疗方案无关。结论:在经典的MTS1A中,SV2亚型的表达发生了变化,其中SV2A和SV2B显着降低,与突触损失平行,而SV2C在发芽的苔藓纤维中选择性升高。这些发现暗示了萌发突触的生理机制不同,并且有可能以SV2C特异性策略来针对它们。

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