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Inhibitory postsynaptic membrane specializations are formed in gephyrin-deficient mice.

机译:在缺乏gephyrin的小鼠中形成抑制性突触后膜特化。

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摘要

Gephyrin is a major postsynaptic scaffolding protein at GABAergic and glycinergic inhibitory synapses. Gephyrin-deficient (geph(-/-)) mice die after birth due to disinhibition of motor and sensory pathways resulting from a lack of postsynaptic glycine receptor and GABA(A) receptor clusters. Here, immunoelectron and confocal microscopy revealed that postsynaptic membrane specializations are formed in the absence of gephyrin. First, in brainstem sections obtained from newborn geph(-/-) mice inhibitory nerve terminals identified by immunogold labeling of either the vesicular inhibitory amino acid transporter (VIAAT) or GABA were found to be apposed to postsynaptic membrane areas decorated by electron-dense material. Second, neuroligin-2, a membrane protein of inhibitory postsynapses, was clustered beneath glutamate decarboxylase 65 (GAD-65) positive nerve terminals in geph(-/-) hippocampal cultures. These results indicate that proteins other than gephyrin define the ultrastructure of inhibitory postsynaptic membrane specializations.
机译:卟啉是GABA能和甘氨酸抑制性突触的主要突触后支架蛋白。由于缺乏突触后甘氨酸受体和GABA(A)受体簇而导致运动和感觉途径的抑制,缺乏Gephyrin的(geph(-/-))小鼠在出生后死亡。在这里,免疫电子和共聚焦显微镜显示突触后膜的专业化是在没有gephyrin的情况下形成的。首先,在从新生的geph(-/-)小鼠获得的脑干切片中,通过免疫金标记的囊泡抑制性氨基酸转运蛋白(VIAAT)或GABA鉴定出的抑制性神经末梢被发现与由电子致密材料修饰的突触后膜区域相对应。 。其次,neuroligin-2是一种抑制性突触后的膜蛋白,聚集在geph(-/-)海马培养物中的谷氨酸脱羧酶65(GAD-65)阳性神经末端下方。这些结果表明,除gephyrin以外的蛋白还定义了抑制突触后膜特化的超微结构。

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