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首页> 外文期刊>Neuron >Structured Dendritic Inhibition Supports Branch-Selective Integration in CA1 Pyramidal Cells
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Structured Dendritic Inhibition Supports Branch-Selective Integration in CA1 Pyramidal Cells

机译:结构树突抑制在CA1金字塔形细胞中支持分支选择性整合。

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Neuronal circuit function is governed by precise patterns of connectivity between specialized groups of neurons. The diversity of GABAergic interneurons is a hallmark of cortical circuits, yet little is known about their targeting to individual postsynaptic dendrites. We examined synaptic connectivity between molecularly defined inhibitory interneurons and CA1 pyramidal cell dendrites using correlative light-electron microscopy and large-volume array tomography. We show that interneurons can be highly selective in their connectivity to specific dendritic branch types and, furthermore, exhibit precisely targeted connectivity to the origin or end of individual branches. Computational simulations indicate that the observed subcellular targeting enables control over the nonlinear integration of synaptic input or the initiation and backpropagation of action potentials in a branch-selective manner. Our results demonstrate that connectivity between interneurons and pyramidal cell dendrites is more precise and spatially segregated than previously appreciated, which may be a critical determinant of how inhibition shapes dendritic computation.
机译:神经元回路功能由专门的神经元组之间的连通性的精确模式控制。 GABA能中间神经元的多样性是皮层回路的标志,但对它们靶向单个突触后树突的了解却很少。我们使用相关的光电子显微镜和大容量阵列层析成像技术检查了分子定义的抑制神经元和CA1锥体细胞树突之间的突触连接。我们表明,中间神经元在与特定树突分支类型的连通性方面可以具有高度选择性,此外,还可以精确定位到各个分支的起源或末端的目标连通性。计算模拟表明,观察到的亚细胞靶向能够以分支选择性方式控制突触输入的非线性整合或动作电位的引发和反向传播。我们的结果表明,中间神经元和锥体细胞树突之间的连通性比以前认识到的更为精确和空间隔离,这可能是抑制作用如何影响树突计算的关键决定因素。

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