小鼠皮质-丘脑-皮质驱动和调节回路的互补组织。

IF 4.4 2区 医学 Q1 NEUROSCIENCES
Rachel M Cassidy, Angel V Macias, Willian N Lagos, Chiamaka Ugorji, Edward M Callaway
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引用次数: 0

摘要

视觉系统中的皮质-皮质(CC)投射促进了感觉信息的分层处理。除了直接的皮层-丘脑-皮层(CTC)连接外,通过丘脑枕核的间接皮质-丘脑-皮层(CTC)通路可以根据行为需求传递感觉信号并介导皮层相互作用。虽然枕状核与整个视觉皮层广泛相连,但尚不清楚跨丘脑通路是否连接所有皮层区域,或者它们是否遵循系统的组织规则。由于投射到不同区域的小鼠枕核神经元在空间上是混杂的,它们的输入/输出关系很难用传统的解剖学方法来表征。为了确定CTC电路的组织结构,我们利用固有信号成像技术绘制了雄性和雌性小鼠的高视区(HVA),并针对5条pulvinar→HVA通路进行了狂犬病投影特异性追踪。我们将死后皮层组织与体内图对齐,以精确量化投射到每个pulvinar→HVA群体的区域和细胞类型。第5层皮质丘脑(L5CT)“驱动”输入到枕状核主要来自初级视觉皮层(V1),与中皮层层级一致。来自横向hva的L5CT输入特别避免了驱动相互连接,这与“无强回路”假设相一致。相反,第6层皮质丘脑(L6CT)“调制器”输入分布在各个区域,并偏向于相互连接。与以往对灵长类动物的研究不同,我们发现每个HVA都接受来自上丘的失突触输入。因此,枕状核中的CTC电路取决于目标HVA和输入细胞类型,因此驱动和调制高阶通路遵循类似于控制一阶CT电路的互补连接规则。理解枕后肌的功能需要了解其解剖学联系。使用最先进的狂犬病追踪技术,我们建立了全脑和中枢性脑脊液的连接图。虽然灵长类动物的丘顶神经通路选择性地以背侧视觉区为目标,但我们在小鼠中发现无处不在的SC输入。这种突起外投射支持无意识的视觉引导行为,表明小鼠所有的视觉皮质区域都参与了这种功能。我们的结果也统一了长期存在的解剖学假设。也就是说,“驱动器”CTC输入是前馈继电器,并坚持“无强回路”假设。“调制器”L6CT输入在目标HVA中被过度表示,反映了先前批量跟踪研究中描述的互易连通性。总之,这些发现构成了一个全面的地图,指导未来的实验和理论研究的脉冲星功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Complementary Organization of Mouse Driver and Modulator Cortico-thalamo-cortical Circuits.

Corticocortical (CC) projections in the visual system facilitate hierarchical processing of sensory information. In addition to direct CC connections, indirect cortico-thalamo-cortical (CTC) pathways through the pulvinar nucleus of the thalamus can relay sensory signals and mediate cortical interactions according to behavioral demands. While the pulvinar connects extensively to the entire visual cortex, it is unknown whether transthalamic pathways link all cortical areas or whether they follow systematic organizational rules. Because mouse pulvinar neurons projecting to different areas are spatially intermingled, their input/output relationships have been difficult to characterize using traditional anatomical methods. To determine the organization of CTC circuits, we mapped the higher visual areas (HVAs) of male and female mice with intrinsic signal imaging and targeted five pulvinar→HVA pathways for projection-specific rabies tracing. We aligned postmortem cortical tissue to in vivo maps for precise quantification of the areas and cell types projecting to each pulvinar→HVA population. Layer 5 corticothalamic (L5CT) "driver" inputs to the pulvinar originate predominantly from primary visual cortex (V1), consistent with the CC hierarchy. L5CT inputs from lateral HVAs specifically avoid driving reciprocal connections, consistent with the "no-strong-loops" hypothesis. Conversely, layer 6 corticothalamic (L6CT) "modulator" inputs are distributed across areas and are biased toward reciprocal connections. Unlike previous studies in primates, we find that every HVA receives disynaptic input from the superior colliculus. CTC circuits in the pulvinar thus depend on both target HVA and input cell type, such that driving and modulating higher-order pathways follow complementary connection rules similar to those governing first-order CT circuits.

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来源期刊
Journal of Neuroscience
Journal of Neuroscience 医学-神经科学
CiteScore
9.30
自引率
3.80%
发文量
1164
审稿时长
12 months
期刊介绍: JNeurosci (ISSN 0270-6474) is an official journal of the Society for Neuroscience. It is published weekly by the Society, fifty weeks a year, one volume a year. JNeurosci publishes papers on a broad range of topics of general interest to those working on the nervous system. Authors now have an Open Choice option for their published articles
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