Two-photon calcium imaging of evoked activity from L5 somatosensory neurons in 
vivo

Mittmann, W; Wallace, DJ; Czubayko, U; Herb, JT; Schaefer, AT; Looger, LL; Denk , W; Kerr, JND

doi:10.1038/nn.2879

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Two-photon calcium imaging of evoked activity from L5 somatosensory neurons in vivo

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Mittmann, W
Former Research Group Network Imaging, Max Planck Institute for Biological Cybernetics, Max Planck Society;
Max Planck Institute for Biological Cybernetics, Max Planck Society;

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Wallace, DJ
Former Research Group Network Imaging, Max Planck Institute for Biological Cybernetics, Max Planck Society;
Max Planck Institute for Biological Cybernetics, Max Planck Society;

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Czubayko, U
Former Research Group Network Imaging, Max Planck Institute for Biological Cybernetics, Max Planck Society;
Max Planck Institute for Biological Cybernetics, Max Planck Society;

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Kerr, JND
Former Research Group Network Imaging, Max Planck Institute for Biological Cybernetics, Max Planck Society;
Max Planck Institute for Biological Cybernetics, Max Planck Society;

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https://www.nature.com/articles/nn.2879.pdf
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Citation

Mittmann, W., Wallace, D., Czubayko, U., Herb, J., Schaefer, A., Looger, L., et al. (2011). Two-photon calcium imaging of evoked activity from L5 somatosensory neurons in vivo. Nature Neuroscience, 14(8), 1089-1093. doi:10.1038/nn.2879.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0013-BAC4-B

Abstract

Multiphoton imaging (MPI) is widely used for recording activity simultaneously from many neurons in superficial cortical layers in vivo. We combined regenerative amplification multiphoton microscopy (RAMM) with genetically encoded calcium indicators to extend MPI of neuronal population activity into layer 5 (L5) of adult mouse somatosensory cortex. We found that this approach could be used to record and quantify spontaneous and sensory-evoked activity in populations of L5 neuronal somata located as much as 800 μm below the pia. In addition, we found that RAMM could be used to simultaneously image activity from large (~80) populations of apical dendrites and follow these dendrites down to their somata of origin.