Nature Communications · 2018 · 66 citations · 64 references
Life SciencesNeurobiologyNeuroscienceCellular NeuroscienceNeurophysiologySensory NeuroscienceBrain ImagingCellular ImagingMultiphoton MicroscopyNeural Recording TechnologiesOptical ImagingSuper-resolution MicroscopyCalcium ImagingMultiphoton ImagingNeuroscience ImagingSpontaneous Neural ActivityTwo-photon Fluorescence ImagingTwo-photon Fluorescence MicroscopyTwo-photon MicroscopyWide-field Microscopy
Wide-field imaging of neural activity at a cellular resolution is a current challenge in neuroscience. To address this issue, wide-field two-photon microscopy has been developed; however, the field size is limited by the objective size. Here, we develop a micro-opto-mechanical device that rotates within the post-objective space between the objective and brain tissue. Two-photon microscopy with this device enables sub-second sequential calcium imaging of left and right mouse sensory forelimb areas 6 mm apart. When imaging the rostral and caudal motor forelimb areas (RFA and CFA) 2 mm apart, we found high pairwise correlations in spontaneous activity between RFA and CFA neurons and between an RFA neuron and its putative axons in CFA. While mice performed a sound-triggered forelimb-movement task, the population activity between RFA and CFA covaried across trials, although the field-averaged activity was similar across trials. The micro-opto-mechanical device in the post-objective space provides a novel and flexible design to clarify the correlation structure between distant brain areas at subcellular and population levels.
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