| Literature DB >> 30865900 |
Xiaojun Wang1, Jason Tucciarone2, Siqi Jiang1, Fangfang Yin1, Bor-Shuen Wang3, Dingkang Wang4, Yao Jia1, Xueyan Jia1, Yuxin Li1, Tao Yang1, Zhengchao Xu1, Masood A Akram5, Yusu Wang4, Shaoqun Zeng1, Giorgio A Ascoli5, Partha Mitra3, Hui Gong1, Qingming Luo6, Z Josh Huang7.
Abstract
Parsing diverse nerve cells into biological types is necessary for understanding neural circuit organization. Morphology is an intuitive criterion for neuronal classification and a proxy of connectivity, but morphological diversity and variability often preclude resolving the granularity of neuron types. Combining genetic labeling with high-resolution, large-volume light microscopy, we established a single neuron anatomy platform that resolves, registers, and quantifies complete neuron morphologies in the mouse brain. We discovered that cortical axo-axonic cells (AACs), a cardinal GABAergic interneuron type that controls pyramidal neuron (PyN) spiking at axon initial segments, consist of multiple subtypes distinguished by highly laminar-specific soma position and dendritic and axonal arborization patterns. Whereas the laminar arrangements of AAC dendrites reflect differential recruitment by input streams, the laminar distribution and local geometry of AAC axons enable differential innervation of PyN ensembles. This platform will facilitate genetically targeted, high-resolution, and scalable single neuron anatomy in the mouse brain.Entities:
Keywords: AACs; ChCs; GABAergic interneurons; axo-axonic cells; chandelier cells; fMOST; gSNA; genetic single neuron anatomy; neuron subtypes
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Year: 2019 PMID: 30865900 DOI: 10.1016/j.celrep.2019.02.040
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423