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      Multiphoton imaging of neural structure and activity in Drosophila through the intact cuticle

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          Abstract

          We developed a multiphoton imaging method to capture neural structure and activity in behaving flies through the intact cuticle. Our measurements showed that the fly head cuticle has surprisingly high transmission at wavelengths >900nm, and the difficulty of through-cuticle imaging is due to the air sacs and/or fat tissue underneath the head cuticle. By compressing or removing the air sacs, we performed multiphoton imaging of the fly brain through the intact cuticle. Our anatomical and functional imaging results show that 2- and 3-photon imaging are comparable in superficial regions such as the mushroom body, but 3-photon imaging is superior in deeper regions such as the central complex and beyond. We further demonstrated 2-photon through-cuticle functional imaging of odor-evoked calcium responses from the mushroom body γ-lobes in behaving flies short term and long term. The through-cuticle imaging method developed here extends the time limits of in vivo imaging in flies and opens new ways to capture neural structure and activity from the fly brain.

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          Most cited references53

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          Fiji: an open-source platform for biological-image analysis.

          Fiji is a distribution of the popular open-source software ImageJ focused on biological-image analysis. Fiji uses modern software engineering practices to combine powerful software libraries with a broad range of scripting languages to enable rapid prototyping of image-processing algorithms. Fiji facilitates the transformation of new algorithms into ImageJ plugins that can be shared with end users through an integrated update system. We propose Fiji as a platform for productive collaboration between computer science and biology research communities.
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            Ultra-sensitive fluorescent proteins for imaging neuronal activity

            Summary Fluorescent calcium sensors are widely used to image neural activity. Using structure-based mutagenesis and neuron-based screening, we developed a family of ultra-sensitive protein calcium sensors (GCaMP6) that outperformed other sensors in cultured neurons and in zebrafish, flies, and mice in vivo. In layer 2/3 pyramidal neurons of the mouse visual cortex, GCaMP6 reliably detected single action potentials in neuronal somata and orientation-tuned synaptic calcium transients in individual dendritic spines. The orientation tuning of structurally persistent spines was largely stable over timescales of weeks. Orientation tuning averaged across spine populations predicted the tuning of their parent cell. Although the somata of GABAergic neurons showed little orientation tuning, their dendrites included highly tuned dendritic segments (5 - 40 micrometers long). GCaMP6 sensors thus provide new windows into the organization and dynamics of neural circuits over multiple spatial and temporal scales.
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              In vivo three-photon microscopy of subcortical structures within an intact mouse brain

              Two-photon fluorescence microscopy (2PM) 1 enables scientists in various fields including neuroscience 2,3 , embryology 4 , and oncology 5 to visualize in vivo and ex vivo tissue morphology and physiology at a cellular level deep within scattering tissue. However, tissue scattering limits the maximum imaging depth of 2PM within the mouse brain to the cortical layer, and imaging subcortical structures currently requires the removal of overlying brain tissue 3 or the insertion of optical probes 6,7 . Here we demonstrate non-invasive, high resolution, in vivo imaging of subcortical structures within an intact mouse brain using three-photon fluorescence microscopy (3PM) at a spectral excitation window of 1,700 nm. Vascular structures as well as red fluorescent protein (RFP)-labeled neurons within the mouse hippocampus are imaged. The combination of the long excitation wavelength and the higher order nonlinear excitation overcomes the limitations of 2PM, enabling biological investigations to take place at greater depth within tissue.
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                Author and article information

                Contributors
                Role: Reviewing Editor
                Role: Senior Editor
                Journal
                eLife
                Elife
                eLife
                eLife
                eLife Sciences Publications, Ltd
                2050-084X
                24 January 2022
                2022
                : 11
                : e69094
                Affiliations
                [1 ] Department of Neurobiology and Behavior, Cornell University ( https://ror.org/05bnh6r87) Ithaca United States
                [2 ] School of Applied and Engineering Physics, Cornell University ( https://ror.org/05bnh6r87) Ithaca United States
                [3 ] Department of Physics, University of Florida ( https://ror.org/02y3ad647) Gainesville United States
                Tata Institute of Fundamental Research India
                National Centre for Biological Sciences, Tata Institute of Fundamental Research ( https://ror.org/03ht1xw27) India
                Tata Institute of Fundamental Research India
                Tata Institute of Fundamental Research India
                Author notes
                [†]

                These authors contributed equally to this work.

                [‡]

                Princeton Neuroscience Institute, Princeton University, Princeton, United States.

                Author information
                https://orcid.org/0000-0001-6935-0381
                https://orcid.org/0000-0003-0061-0258
                https://orcid.org/0000-0002-6674-1165
                https://orcid.org/0000-0002-1174-5046
                https://orcid.org/0000-0002-3493-6427
                https://orcid.org/0000-0002-1130-5083
                Article
                69094
                10.7554/eLife.69094
                8846588
                35073257
                4a2c92f5-afe4-4b93-842f-35536dde6a8b
                © 2022, Aragon et al

                This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

                History
                : 04 April 2021
                : 23 January 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100000001, National Science Foundation;
                Award ID: DBI-1707312
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000057, National Institute of General Medical Sciences;
                Award ID: R35 GM133698
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000875, Pew Charitable Trusts;
                Award ID: Scholars Award
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000879, Alfred P. Sloan Foundation;
                Award ID: Scholars Award
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000965, American Federation for Aging Research;
                Award ID: Grants for Junior Faculty
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000001, NSF NeuroNex Program;
                Award ID: DBI-1707312
                Award Recipient :
                The funders had no role in study design, data collection, and interpretation, or the decision to submit the work for publication.
                Categories
                Tools and Resources
                Neuroscience
                Custom metadata
                Development of imaging methods to capture neural activity and structure through the intact cuticle using 2-photon and 3-photon excitation in the genetic model organism, Drosophila melanogaster.

                Life sciences
                multiphoton imaging,olfaction,behavior,drosophila melanogaster
                Life sciences
                multiphoton imaging, olfaction, behavior, drosophila melanogaster

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