首页> 美国卫生研究院文献>eNeuro >Metaplastic Regulation of CA1 Schaffer Collateral Pathway Plasticity by Hebbian MGluR1a-Mediated Plasticity at Excitatory Synapses onto Somatostatin-Expressing Interneurons
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Metaplastic Regulation of CA1 Schaffer Collateral Pathway Plasticity by Hebbian MGluR1a-Mediated Plasticity at Excitatory Synapses onto Somatostatin-Expressing Interneurons

机译:由Hebbian MGluR1a介导的可塑性表达促生长素的中间神经元在兴奋性突触中的CA1 Schaffer旁通路可塑性的代谢调控。

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摘要

Cortical GABAergic interneurons represent a highly diverse neuronal type that regulates neural network activity. In particular, interneurons in the hippocampal CA1 oriens/alveus (O/A-INs) area provide feedback dendritic inhibition to local pyramidal cells and express somatostatin (SOM). Under relevant afferent stimulation patterns, they undergo long-term potentiation (LTP) of their excitatory synaptic inputs through multiple induction and expression mechanisms. However, the cell-type specificity of these different forms of LTP and their specific contribution to the dynamic regulation of the CA1 network remain unclear. Here we recorded from SOM-expressing interneurons (SOM-INs) in the O/A region from SOM-Cre-Ai3 transgenic mice in whole-cell patch-clamp. Results indicate that, like in anatomically identified O/A-INs, theta-burst stimulation (TBS) induced a Hebbian form of LTP dependent on metabotropic glutamate receptor type 1a (mGluR1a) in SOM-INs, but not in parvalbumin-expressing interneurons, another mainly nonoverlapping interneuron subtype in CA1. In addition, we demonstrated using field recordings from transgenic mice expressing archaerhodopsin 3 selectively in SOM-INs, that a prior conditioning TBS in O/A, to induce mGluR1a-dependent LTP in SOM-INs, upregulated LTP in the Schaffer collateral pathway of pyramidal cells. This effect was prevented by light-induced hyperpolarization of SOM-INs during TBS, or by application of the mGluR1a antagonist , indicating a necessity for mGluR1a and SOM-INs activation. These results uncover that SOM-INs perform an activity-dependent metaplastic control on hippocampal CA1 microcircuits in a cell-specific fashion. Our findings provide new insights on the contribution of interneuron synaptic plasticity in the regulation of the hippocampal network activity and mnemonic processes.
机译:皮质GABA能中间神经元代表高度多样化的神经元类型,可调节神经网络活动。特别是,海马CA1区/肺泡(O / A-INs)区域中的中间神经元为局部锥体细胞提供反馈树突抑制并表达生长抑素(SOM)。在相关的传入刺激模式下,它们通过多种诱导和表达机制对其兴奋性突触输入进行长期增强(LTP)。但是,这些不同形式的LTP的细胞类型特异性及其对CA1网络动态调节的特定作用仍不清楚。在这里,我们在全细胞膜片钳中从SOM-Cre-Ai3转基因小鼠的O / A区中的SOM表达中间神经元(SOM-IN)记录下来。结果表明,就像在解剖学上确定的O / A-INs一样,theta-burst刺激(TBS)诱导了Hebbian形式的LTP,它依赖于SOM-INs中的代谢型谷氨酸受体1a(mGluR1a),但不表达小白蛋白的中间神经元, CA1中的另一种主要不重叠的中间神经元亚型。此外,我们证明了使用来自在SOM-INs中选择性表达古细菌视紫红质3的转基因小鼠的现场记录,证明在O / A中预先调节TBS可以诱导SOM-INs中依赖mGluR1a的LTP,在锥体的Schaffer侧支途径中上调LTP细胞。在TBS期间通过光诱导SOM-INs的超极化或通过应用mGluR1a拮抗剂(表明需要激活mGluR1a和SOM-INs)可以防止此作用。这些结果表明,SOM-INs以细胞特异性方式对海马CA1微电路执行了活动依赖性的化生控制。我们的发现为神经元突触可塑性在调节海马网络活动和助记过程中的作用提供了新的见解。

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