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Nat Neurosci. 2017 Apr;20(4):620-628. doi: 10.1038/nn.4516. Epub 2017 Feb 27.

Video-rate volumetric functional imaging of the brain at synaptic resolution.

Author information

1
Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, Virginia, USA.
2
Champalimaud Neuroscience Programme, Champalimaud Centre for the Unknown, Lisbon, Portugal.
3
Center of Advanced European Studies and Research, Bonn, Germany.
4
Department of Functional Architecture and Development of Cerebral Cortex, Max Planck Florida Institute for Neuroscience, Jupiter, Florida, USA.
5
Division of Biological Science, Graduate School of Science, Nagoya University, Nagoya, Japan.

Abstract

Neurons and neural networks often extend hundreds of micrometers in three dimensions. Capturing the calcium transients associated with their activity requires volume imaging methods with subsecond temporal resolution. Such speed is a challenge for conventional two-photon laser-scanning microscopy, because it depends on serial focal scanning in 3D and indicators with limited brightness. Here we present an optical module that is easily integrated into standard two-photon laser-scanning microscopes to generate an axially elongated Bessel focus, which when scanned in 2D turns frame rate into volume rate. We demonstrated the power of this approach in enabling discoveries for neurobiology by imaging the calcium dynamics of volumes of neurons and synapses in fruit flies, zebrafish larvae, mice and ferrets in vivo. Calcium signals in objects as small as dendritic spines could be resolved at video rates, provided that the samples were sparsely labeled to limit overlap in their axially projected images.

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PMID:
28250408
PMCID:
PMC5374000
DOI:
10.1038/nn.4516
[Indexed for MEDLINE]
Free PMC Article

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