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Astrocytes detect and upregulate transmission at inhibitory synapses of somatostatin interneurons onto pyramidal cells

机译:星形胶质细胞检测和抑制生长抑素中间神经元突触向锥体细胞的传递。

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摘要

Astrocytes are important regulators of excitatory synaptic networks. However, astrocytes regulation of inhibitory synaptic systems remains ill defined. This is particularly relevant since GABAergic interneurons regulate the activity of excitatory cells and shape network function. To address this issue, we combined optogenetics and pharmacological approaches, two-photon confocal imaging and whole-cell recordings to specifically activate hippocampal somatostatin or paravalbumin-expressing interneurons (SOM-INs or PV-INs), while monitoring inhibitory synaptic currents in pyramidal cells and Ca2+ responses in astrocytes. We found that astrocytes detect SOM-IN synaptic activity via GABABR and GAT-3-dependent Ca2+ signaling mechanisms, the latter triggering the release of ATP. In turn, ATP is converted into adenosine, activating A1Rs and upregulating SOM-IN synaptic inhibition of pyramidal cells, but not PV-IN inhibition. Our findings uncover functional interactions between a specific subpopulation of interneurons, astrocytes and pyramidal cells, involved in positive feedback autoregulation of dendritic inhibition of pyramidal cells.
机译:星形胶质细胞是兴奋性突触网络的重要调节剂。然而,星形胶质细胞对抑制性突触系统的调节仍然不清楚。这一点特别重要,因为GABA能的中间神经元调节兴奋性细胞的活性和形状网络功能。为了解决这个问题,我们结合了光遗传学和药理学方法,双光子共聚焦成像和全细胞记录,以专门激活海马生长抑素或表达副白蛋白的中间神经元(SOM-IN或PV-IN),同时监测锥体细胞的抑制性突触电流。和星形胶质细胞中的Ca 2 + 反应。我们发现星形胶质细胞通过GABABR和依赖GAT-3的Ca 2 + 信号传导机制检测SOM-IN突触活性,后者触发ATP的释放。反过来,ATP转换为腺苷,激活A1Rs,并上调锥体细胞的SOM-IN突触抑制,但不上调PV-IN抑制。我们的发现揭示了中间神经元,星形胶质细胞和锥体细胞的特定亚群之间的功能相互作用,涉及锥体细胞对树突状抑制的正反馈自动调节。

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