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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Target-cell-specific left-right asymmetry of NMDA receptor content in schaffer collateral synapses in epsilon1/NR2A knock-out mice.
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Target-cell-specific left-right asymmetry of NMDA receptor content in schaffer collateral synapses in epsilon1/NR2A knock-out mice.

机译:在epsilon1 / NR2A基因敲除小鼠的沙弗氏侧突触中NMDA受体含量的靶细胞特异性左右不对称性。

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Input-dependent left-right asymmetry of NMDA receptor epsilon2 (NR2B) subunit allocation was discovered in hippocampal Schaffer collateral (Sch) and commissural fiber pyramidal cell synapses (Kawakami et al., 2003). To investigate whether this asymmetrical epsilon2 allocation is also related to the types of the postsynaptic cells, we compared postembedding immunogold labeling for epsilon2 in left and right Sch synapses on pyramidal cells and interneurons. To facilitate the detection of epsilon2 density difference, we used epsilon1 (NR2A) knock-out (KO) mice, which have a simplified NMDA receptor subunit composition. The labeling density for epsilon2 but not zeta1 (NR1) and subtype 2/3 glutamate receptor (GluR2/3) in Sch-CA1 pyramidal cell synapses was significantly different between the left and right hippocampus with opposite directions in strata oriens and radiatum; the left to right ratio of epsilon2 labeling density was 1:1.50 in stratum oriens and 1.44:1 in stratum radiatum. No significant difference, however, was detected in CA1 stratum radiatum between the left and right Sch-GluR4-positive (mostly parvalbumin-positive) and Sch-GluR4-negative interneuron synapses. Consistent with the anatomical asymmetry, the amplitude ratio of NMDA EPSCs to non-NMDA EPSCs in pyramidal cells was approximately two times larger in right than left stratum radiatum and vice versa in stratum oriens of epsilon1 KO mice. Moreover, the amplitude of long-term potentiation in the Sch-CA1 synapses of left stratum radiatum was significantly larger than that in the right corresponding synapses. These results indicate that the asymmetry of epsilon2 distribution is target cell specific, resulting in the left-right difference in NMDA receptor content and plasticity in Sch-CA1 pyramidal cell synapses in epsilon1 KO mice.
机译:在海马Schaffer侧支(Sch)和连合纤维锥体细胞突触中发现了NMDA受体ε2(NR2B)亚单位分配的输入依赖的左右不对称性(Kawakami et al。,2003)。为了研究这种不对称的epsilon2分配是否也与突触后细胞的类型有关,我们比较了锥体细胞和中间神经元的左右Sch突触中epsilon2的包埋后免疫金标记。为了便于检测epsilon2密度差异,我们使用了具有简化的NMDA受体亚基组成的epsilon1(NR2A)敲除(KO)小鼠。在左海马和右海马中,ε-二环的sepsilon2的标记密度而不是zeta1(NR1)和2/3型谷氨酸受体(GluR2 / 3)的标记密度显着不同,而在左和右海马之间的方向相反。 epsilon2标记密度的左右比率在东方层中为1:1.50,在放射状层中为1.44:1。然而,在左右Sch-GluR4阳性(主要是小白蛋白阳性)和Sch-GluR4阴性的中间神经元突触之间的CA1层半径中未检测到显着差异。与解剖学上的不对称一致,锥体细胞中NMDA EPSC与非NMDA EPSC的振幅比在右侧比在epsilon1 KO小鼠的左侧层半径大两倍,反之亦然。此外,左侧层放射状的Sch-CA1突触的长期增强幅度明显大于右侧相应突触的长期增强幅度。这些结果表明,epsilon2分布的不对称性是靶细胞特异性的,导致epsilon1 KO小鼠的NMDA受体含量和Sch-CA1锥体细胞突触的可塑性具有左右差异。

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