| Literature DB >> 28009304 |
Tony Hyun Kim1, Yanping Zhang2, Jérôme Lecoq3, Juergen C Jung1, Jane Li4, Hongkui Zeng5, Cristopher M Niell6, Mark J Schnitzer7.
Abstract
A major technological goal in neuroscience is to enable the interrogation of individual cells across the live brain. By creating a curved glass replacement to the dorsal cranium and surgical methods for its installation, we developed a chronic mouse preparation providing optical access to an estimated 800,000-1,100,000 individual neurons across the dorsal surface of neocortex. Post-surgical histological studies revealed comparable glial activation as in control mice. In behaving mice expressing a Ca2+ indicator in cortical pyramidal neurons, we performed Ca2+ imaging across neocortex using an epi-fluorescence macroscope and estimated that 25,000-50,000 individual neurons were accessible per mouse across multiple focal planes. Two-photon microscopy revealed dendritic morphologies throughout neocortex, allowed time-lapse imaging of individual cells, and yielded estimates of >1 million accessible neurons per mouse by serial tiling. This approach supports a variety of optical techniques and enables studies of cells across >30 neocortical areas in behaving mice.Entities:
Keywords: brain imaging; calcium imaging; dendrites; dendritic spines; fluorescence imaging; mouse behavior; neocortex; neural ensembles; two-photon microscopy
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Year: 2016 PMID: 28009304 PMCID: PMC5459490 DOI: 10.1016/j.celrep.2016.12.004
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423