首页> 美国卫生研究院文献>The Journal of Neuroscience >Several types of Ca2+ channels mediate glutamatergic synaptic responses to activation of single Thy-1-immunolabeled rat retinal ganglion neurons
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Several types of Ca2+ channels mediate glutamatergic synaptic responses to activation of single Thy-1-immunolabeled rat retinal ganglion neurons

机译:几种类型的Ca2 +通道介导谷氨酸能突触对Thy-1-免疫标记的大鼠视网膜神经节神经元激活的反应。

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摘要

A dissociated cell culture from the postnatal rat retina was established to characterize the synapses formed by retinal ganglion neurons (RGNs) in vitro. An antibody against Thy-1.1 was used to preselect putative RGNs for pair patch-clamp recording with the principal aim of identifying the released transmitter(s) and estimating the role of different types of voltage-activated Ca2+ channels in evoked transmitter release. The population of Thy-1+ neurons was heterogeneous. Staining patterns, soma-dendritic geometries and axon length displayed variations that could be related to basic electrophysiological properties, such as amplitudes of voltage- activated Na+ currents (INa(V)), action potential size and capacity for repetitive discharge. Out of 73 coupled connections, 33 pairs were glutamatergic. With no exception, these connections were formed by the axons of strongly labeled Thy-1+ neurons with large INa(V) (typically > 2 nA) and repetitive firing over a broad current range. Such neurons were classified as RGNs. Forty out of 73 coupled pairs were GABAergic. These connections were always formed by weakly stained Thy-1+ neurons with small INa(V) (typically < 2 nA) and very limited capacity for repetitive discharge. Such neurons were tentatively classified as displaced amacrine cells. Evoked EPSCs in response to RGN activation were completely blocked by low concentrations of Cd2+ or Gd3+. omega- CgTx-GVIA (5 microM) reduced EPSCs to 67 +/- 29%, omega-AgaTx-IVA (200 nM) had no effect, and nifedipine (15 microM) enhanced the evoked EPSCs. Our experiments indicate that (1) the transmitter released by RGNs is glutamate and (2) the major part of synaptic glutamate release is governed by a novel toxin-resistant Ca2+ channel. The results further suggest that the characteristic phenotype of RGNs is well maintained in dissociated cell culture. In conjunction with electrophysiological tests Thy-1+ labeling can be used for RGN identification.
机译:建立了从产后大鼠视网膜分离的细胞培养物,以表征体外视网膜神经节神经元(RGN)形成的突触。抗Thy-1.1的抗体被用于预选择推定的RGN,用于成对膜片钳记录,其主要目的是鉴定释放的发射器,并估计不同类型的电压激活的Ca2 +通道在诱发的发射器释放中的作用。 Thy-1 +神经元的种群是异质的。染色模式,树突状体的几何形状和轴突长度显示出可能与基本电生理特性有关的变化,例如电压激活的Na +电流(INa(V))的幅度,动作电位的大小和重复放电的能力。在73对偶合的连接中,有33对是谷氨酸能的。毫无例外,这些连接是由带有强INa(V)(通常> 2 nA)的强标记Thy-1 +神经元的轴突和在很宽的电流范围内重复发射形成的。这些神经元被分类为RGN。 73对偶合中有40对为GABA能。这些连接始终是由染色小的Thy-1 +神经元形成的,这些Thy-1 +神经元的INa(V)小(通常<2 nA),并且重复放电的能力非常有限。暂时将这类神经元分类为置换的无长突细胞。低浓度的Cd2 +或Gd3 +完全阻止了响应RGN激活的诱发EPSC。 ω-CgTx-GVIA(5 microM)将EPSC降至67 +/- 29%,ω-AgaTx-IVA(200 nM)没有作用,而硝苯地平(15 microM)增强了诱发的EPSC。我们的实验表明,(1)RGNs释放的递质是谷氨酸,(2)突触谷氨酸释放的主要部分由新型的抗毒素Ca2 +通道控制。结果进一步表明,RGNs的特征表型在分离的细胞培养物中得到了很好的维持。结合电生理测试,Thy-1 +标记可用于RGN鉴定。

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