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( A ) Schematic of excitatory cortical projection neuron subtypes (left). Representative coronal sections of ACtx showing GCaMP8s expression (green) and 4′,6-diamidino-2-phenylindole (DAPI)–labeled (blue) nuclei (right). The transgenic and viral strategies noted in (B) were used to target L2/3, L5 IT, L5 ET, or CT neurons. WM, white matter. Scale bar, 250 μm. ( B ) Overview of the experimental design. Mice passively listen to pure tone frequencies, <t>while</t> <t>two-photon</t> calcium imaging and pupillometry were performed simultaneously. Cell-type–specific targeting strategies (top) used a combination of viral and/or transgenic methods. WT, wild type. Exemplar two-photon fields of view (FOVs) of each target ACtx cell subpopulation (right). Scale bar, 250 μm. ( C ) Exemplar 5-min recording showing pupil diameter (top; black), deconvolved neural activity from a single ET neuron (middle; orange), and sound onset times (bottom). Pupil size is expressed as a percentage of maximum diameter; neural activity is plotted in SDs ( z -scored) from baseline. ( D ) Histogram of trialwise pupil states across all mice. Counts refer to number of trials. Median pupil size of 62% is denoted by the yellow dashed line.
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( A ) Schematic of excitatory cortical projection neuron subtypes (left). Representative coronal sections of ACtx showing GCaMP8s expression (green) and 4′,6-diamidino-2-phenylindole (DAPI)–labeled (blue) nuclei (right). The transgenic and viral strategies noted in (B) were used to target L2/3, L5 IT, L5 ET, or CT neurons. WM, white matter. Scale bar, 250 μm. ( B ) Overview of the experimental design. Mice passively listen to pure tone frequencies, <t>while</t> <t>two-photon</t> calcium imaging and pupillometry were performed simultaneously. Cell-type–specific targeting strategies (top) used a combination of viral and/or transgenic methods. WT, wild type. Exemplar two-photon fields of view (FOVs) of each target ACtx cell subpopulation (right). Scale bar, 250 μm. ( C ) Exemplar 5-min recording showing pupil diameter (top; black), deconvolved neural activity from a single ET neuron (middle; orange), and sound onset times (bottom). Pupil size is expressed as a percentage of maximum diameter; neural activity is plotted in SDs ( z -scored) from baseline. ( D ) Histogram of trialwise pupil states across all mice. Counts refer to number of trials. Median pupil size of 62% is denoted by the yellow dashed line.
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Image Search Results


( A ) Schematic of excitatory cortical projection neuron subtypes (left). Representative coronal sections of ACtx showing GCaMP8s expression (green) and 4′,6-diamidino-2-phenylindole (DAPI)–labeled (blue) nuclei (right). The transgenic and viral strategies noted in (B) were used to target L2/3, L5 IT, L5 ET, or CT neurons. WM, white matter. Scale bar, 250 μm. ( B ) Overview of the experimental design. Mice passively listen to pure tone frequencies, while two-photon calcium imaging and pupillometry were performed simultaneously. Cell-type–specific targeting strategies (top) used a combination of viral and/or transgenic methods. WT, wild type. Exemplar two-photon fields of view (FOVs) of each target ACtx cell subpopulation (right). Scale bar, 250 μm. ( C ) Exemplar 5-min recording showing pupil diameter (top; black), deconvolved neural activity from a single ET neuron (middle; orange), and sound onset times (bottom). Pupil size is expressed as a percentage of maximum diameter; neural activity is plotted in SDs ( z -scored) from baseline. ( D ) Histogram of trialwise pupil states across all mice. Counts refer to number of trials. Median pupil size of 62% is denoted by the yellow dashed line.

Journal: Science Advances

Article Title: Pupil-linked arousal heterogeneously modulates cell-type–specific sensory processing

doi: 10.1126/sciadv.adz6495

Figure Lengend Snippet: ( A ) Schematic of excitatory cortical projection neuron subtypes (left). Representative coronal sections of ACtx showing GCaMP8s expression (green) and 4′,6-diamidino-2-phenylindole (DAPI)–labeled (blue) nuclei (right). The transgenic and viral strategies noted in (B) were used to target L2/3, L5 IT, L5 ET, or CT neurons. WM, white matter. Scale bar, 250 μm. ( B ) Overview of the experimental design. Mice passively listen to pure tone frequencies, while two-photon calcium imaging and pupillometry were performed simultaneously. Cell-type–specific targeting strategies (top) used a combination of viral and/or transgenic methods. WT, wild type. Exemplar two-photon fields of view (FOVs) of each target ACtx cell subpopulation (right). Scale bar, 250 μm. ( C ) Exemplar 5-min recording showing pupil diameter (top; black), deconvolved neural activity from a single ET neuron (middle; orange), and sound onset times (bottom). Pupil size is expressed as a percentage of maximum diameter; neural activity is plotted in SDs ( z -scored) from baseline. ( D ) Histogram of trialwise pupil states across all mice. Counts refer to number of trials. Median pupil size of 62% is denoted by the yellow dashed line.

Article Snippet: All two-photon imaging (Bergamo, Thorlabs) was of the right ACtx.

Techniques: Expressing, Labeling, Transgenic Assay, Imaging, Activity Assay