Mapping astrocyte activity domains by light sheet imaging and spatio-temporal correlation screening

Astrocytes are a major type of glial cell in the mammalian brain, essentially regulating neuronal development and function. Quantitative imaging represents an important approach to study astrocytic signaling in neural circuits. Focusing on astrocytic Ca2+ activity, a key pathway implicated in astrocye-neuron interaction, we here report a strategy combining fast light sheet fluorescence microscopy (LSFM) and correlative screening-based time series analysis, to map activity domains in astrocytes in living mammalian nerve tissue. Light sheet of micron-scale thickness enables wide-field optical sectioning to image astrocytes in acute mouse brain slices. Using both chemical and genetically encoded Ca2+ indicators, we demonstrate the complementary advantages of LSFM in mapping Ca2+ domains in astrocyte populations as compared to epifluorescence and two-photon microscopy. Our approach then revealed distinct kinetics of Ca2+ signals in cortical and hypothalamic astrocytes in resting conditions and following the activation of adrenergic G protein coupled receptor (GPCR). This observation highlights the activity heterogeneity across regionally distinct astrocyte populations, and indicates the potential of our method for investigating dynamic signals in astrocytes.

[1]  Liangyi Chen,et al.  Large-field high-resolution two-photon digital scanned light-sheet microscopy , 2014, Cell Research.

[2]  Bruno Weber,et al.  Cortical Circuit Activity Evokes Rapid Astrocyte Calcium Signals on a Similar Timescale to Neurons , 2018, Neuron.

[3]  Yue Wang,et al.  Automated Functional Analysis of Astrocytes from Chronic Time-Lapse Calcium Imaging Data , 2017, Front. Neuroinform..

[4]  Zhen Chai,et al.  Cellular mechanism for spontaneous calcium oscillations in astrocytes , 2006, Acta Pharmacologica Sinica.

[5]  K. Deisseroth,et al.  Astrocytes Control Breathing Through pH-Dependent Release of ATP , 2010, Science.

[6]  Heping Cheng,et al.  Fast high-resolution miniature two-photon microscopy for brain imaging in freely behaving mice , 2017, Nature Methods.

[7]  Maiken Nedergaard,et al.  Fluorescent Ca2+ indicators directly inhibit the Na,K-ATPase and disrupt cellular functions , 2018, Science Signaling.

[8]  Khaleel Bhaukaurally,et al.  Local Ca2+ detection and modulation of synaptic release by astrocytes , 2011, Nature Neuroscience.

[9]  Stefan R. Pulver,et al.  Ultra-sensitive fluorescent proteins for imaging neuronal activity , 2013, Nature.

[10]  Jin U. Kang,et al.  Norepinephrine Controls Astroglial Responsiveness to Local Circuit Activity , 2014, Neuron.

[11]  Misha B. Ahrens,et al.  Visualizing Whole-Brain Activity and Development at the Single-Cell Level Using Light-Sheet Microscopy , 2015, Neuron.

[12]  G. Buzsáki,et al.  Calcium Dynamics of Cortical Astrocytic Networks In Vivo , 2004, PLoS biology.

[13]  Luke D Lavis,et al.  Synthetic and genetically encoded fluorescent neural activity indicators , 2018, Current Opinion in Neurobiology.

[14]  D. Rowitch,et al.  Functional diversity of astrocytes in neural circuit regulation , 2016, Nature Reviews Neuroscience.

[15]  Stefan R. Pulver,et al.  Genetically encoded calcium indicators for multi-color neural activity imaging and combination with optogenetics , 2013, Front. Mol. Neurosci..

[16]  Eduardo D. Martín,et al.  Synapse-specific astrocyte gating of amygdala-related behavior , 2017, Nature Neuroscience.

[17]  Nicolas Liaudet,et al.  Three-dimensional Ca2+ imaging advances understanding of astrocyte biology , 2017, Science.

[18]  Boudewijn van der Sanden,et al.  Specific In Vivo Staining of Astrocytes in the Whole Brain after Intravenous Injection of Sulforhodamine Dyes , 2012, PloS one.

[19]  Martin Oheim,et al.  Two-photon imaging induces brain heating and calcium microdomain hyperactivity in cortical astrocytes , 2018, bioRxiv.

[20]  Todd A Fiacco,et al.  Multiple Lines of Evidence Indicate That Gliotransmission Does Not Occur under Physiological Conditions , 2018, The Journal of Neuroscience.

[21]  Jonas Frisén,et al.  Transgenic mice for conditional gene manipulation in astroglial cells , 2007, Glia.

[22]  Hans-Ulrich Dodt,et al.  Light sheet microscopy of living or cleared specimens , 2012, Current Opinion in Neurobiology.

[23]  Yutaka Suzuki,et al.  Layer-specific morphological and molecular differences in neocortical astrocytes and their dependence on neuronal layers , 2018, Nature Communications.

[24]  Andrea Volterra,et al.  Astrocyte function from information processing to cognition and cognitive impairment , 2019, Nature Neuroscience.

[25]  M. Nedergaard,et al.  Artifact versus reality—How astrocytes contribute to synaptic events , 2012, Glia.

[26]  Jason R Swedlow,et al.  Quantitative fluorescence microscopy and image deconvolution. , 2007, Methods in cell biology.

[27]  Michael Broxton,et al.  SPED Light Sheet Microscopy: Fast Mapping of Biological System Structure and Function , 2015, Cell.

[28]  Mayeul Collot,et al.  Calcium dynamics in astrocyte processes during neurovascular coupling , 2014, Nature Neuroscience.

[29]  S. Jacques Optical properties of biological tissues: a review , 2013, Physics in medicine and biology.

[30]  Quan Tian,et al.  Recovery from tachyphylaxis of TRPV1 coincides with recycling to the surface membrane , 2019, Proceedings of the National Academy of Sciences.

[31]  F. Helmchen,et al.  Sulforhodamine 101 as a specific marker of astroglia in the neocortex in vivo , 2004, Nature Methods.

[32]  Nicole V. DelRosso,et al.  Accurate quantification of astrocyte and neurotransmitter fluorescence dynamics for single-cell and population-level physiology , 2019, Nature Neuroscience.

[33]  J. Huisken,et al.  A guide to light-sheet fluorescence microscopy for multiscale imaging , 2017, Nature Methods.

[34]  Alfonso Araque,et al.  Neuronal activity determines distinct gliotransmitter release from a single astrocyte , 2018, eLife.

[35]  Raghuveer Parthasarathy,et al.  Comparing phototoxicity during the development of a zebrafish craniofacial bone using confocal and light sheet fluorescence microscopy techniques , 2013, Journal of biophotonics.

[36]  Petra Schwille,et al.  Excitation spectra and brightness optimization of two-photon excited probes. , 2012, Biophysical journal.

[37]  Denis Wirtz,et al.  Transient Opening of the Mitochondrial Permeability Transition Pore Induces Microdomain Calcium Transients in Astrocyte Processes , 2017, Neuron.

[38]  Sharmila Venugopal,et al.  Ca2+ signaling in astrocytes from IP3R2−/− mice in brain slices and during startle responses in vivo , 2015, Nature Neuroscience.

[39]  Y. Xing,et al.  A Transcriptome Database for Astrocytes, Neurons, and Oligodendrocytes: A New Resource for Understanding Brain Development and Function , 2008, The Journal of Neuroscience.

[40]  C. James,et al.  Single objective light-sheet microscopy for high-speed whole-cell 3D super-resolution. , 2016, Biomedical optics express.

[41]  Baljit S. Khakh,et al.  A genetically encoded single-wavelength sensor for imaging cytosolic and cell surface ATP , 2018, Nature Communications.

[42]  Andrea Volterra,et al.  Gliotransmission: Beyond Black-and-White , 2018, The Journal of Neuroscience.

[43]  Nathan C. Klapoetke,et al.  Transgenic Mice for Intersectional Targeting of Neural Sensors and Effectors with High Specificity and Performance , 2015, Neuron.

[44]  Anlian Qu,et al.  Three-dimensional tracking of single secretory granules in live PC12 cells. , 2004, Biophysical journal.

[45]  Alexander Calder The High Sign , 1944 .

[46]  Martin Oheim,et al.  Quantitative Colocalisation Imaging: Concepts, Measurements, and Pitfalls , 2007 .

[47]  Nathalie Rouach,et al.  Versatile control of synaptic circuits by astrocytes: where, when and how? , 2018, Nature Reviews Neuroscience.

[48]  Loren L Looger,et al.  Dysfunctional Calcium and Glutamate Signaling in Striatal Astrocytes from Huntington's Disease Model Mice , 2016, The Journal of Neuroscience.

[49]  J. J. Macklin,et al.  High-performance calcium sensors for imaging activity in neuronal populations and microcompartments , 2019, Nature Methods.

[50]  V. Prévot,et al.  The special relationship: glia–neuron interactions in the neuroendocrine hypothalamus , 2018, Nature Reviews Endocrinology.

[51]  B. Khakh,et al.  Astrocyte calcium signaling: from observations to functions and the challenges therein. , 2015, Cold Spring Harbor perspectives in biology.

[52]  R. Mann,et al.  Swept confocally-aligned planar excitation (SCAPE) microscopy for high speed volumetric imaging of behaving organisms , 2014, Nature Photonics.

[53]  Baljit S Khakh,et al.  A genetically targeted optical sensor to monitor calcium signals in astrocyte processes , 2010, Nature Neuroscience.

[54]  D. Attwell,et al.  Astrocyte calcium signaling: the third wave , 2016, Nature Neuroscience.

[55]  Martin D. Haustein,et al.  Imaging calcium microdomains within entire astrocyte territories and endfeet with GCaMPs expressed using adeno-associated viruses , 2013, The Journal of general physiology.

[56]  M. Ohkura,et al.  A high signal-to-noise Ca2+ probe composed of a single green fluorescent protein , 2001, Nature Biotechnology.

[57]  Todd A Fiacco,et al.  Selective Stimulation of Astrocyte Calcium In Situ Does Not Affect Neuronal Excitatory Synaptic Activity , 2007, Neuron.

[58]  Baljit S Khakh,et al.  Bulk Loading of Calcium Indicator Dyes to Study Astrocyte Physiology: Key Limitations and Improvements Using Morphological Maps , 2011, The Journal of Neuroscience.

[59]  Giovanni Coppola,et al.  Neural Circuit-Specialized Astrocytes: Transcriptomic, Proteomic, Morphological, and Functional Evidence , 2017, Neuron.

[60]  R. Tsien,et al.  Circular permutation and receptor insertion within green fluorescent proteins. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[61]  Kenji F Tanaka,et al.  Role of Purinergic Receptor P2Y1 in Spatiotemporal Ca2+ Dynamics in Astrocytes , 2018, The Journal of Neuroscience.

[62]  Jonathan A. Coles,et al.  Two-photon imaging , 2009 .

[63]  Eduardo D. Martín,et al.  Structural and Functional Plasticity of Astrocyte Processes and Dendritic Spine Interactions , 2014, The Journal of Neuroscience.

[64]  Maiken Nedergaard,et al.  α1-Adrenergic receptors mediate coordinated Ca2+ signaling of cortical astrocytes in awake, behaving mice. , 2013, Cell calcium.

[65]  F. Windels,et al.  Neuronal activity , 2006, Molecular Neurobiology.

[66]  Jason R Swedlow,et al.  Quantitative fluorescence microscopy and image deconvolution. , 2013, Methods in cell biology.

[67]  Karel Svoboda,et al.  ScanImage: Flexible software for operating laser scanning microscopes , 2003, Biomedical engineering online.

[68]  Ilaria Belluomo,et al.  Astroglial CB1 Receptors Determine Synaptic D-Serine Availability to Enable Recognition Memory , 2018, Neuron.

[69]  Willy Supatto,et al.  Whole-brain functional imaging with two-photon light-sheet microscopy , 2015, Nature Methods.

[70]  E. Isacoff,et al.  Optogenetic activation of LiGluR‐expressing astrocytes evokes anion channel‐mediated glutamate release , 2012, The Journal of physiology.

[71]  K. Svoboda,et al.  Principles of Two-Photon Excitation Microscopy and Its Applications to Neuroscience , 2006, Neuron.

[72]  Alan P. Koretsky,et al.  Synchronized Astrocytic Ca2+ Responses in Neurovascular Coupling during Somatosensory Stimulation and for the Resting State , 2018, Cell reports.

[73]  Eduardo D. Martín,et al.  Confocal microscopy for astrocyte in vivo imaging: Recycle and reuse in microscopy , 2013, Front. Cell. Neurosci..

[74]  Shaoqun Zeng,et al.  Photostimulation of astrocytes with femtosecond laser pulses. , 2009, Optics express.

[75]  N. Matsuki,et al.  Large-Scale Calcium Waves Traveling through Astrocytic Networks In Vivo , 2011, The Journal of Neuroscience.

[76]  Andrea Volterra,et al.  Studying Axon-Astrocyte Functional Interactions by 3D Two-Photon Ca2+ Imaging: A Practical Guide to Experiments and “Big Data” Analysis , 2018, Front. Cell. Neurosci..

[77]  Todd A Fiacco,et al.  What Is the Role of Astrocyte Calcium in Neurophysiology? , 2008, Neuron.

[78]  Ulrich Kubitscheck,et al.  Light Sheet Microscopy for Single Molecule Tracking in Living Tissue , 2010, PloS one.

[79]  L. Roux,et al.  Over Astroglial Networks: a Step Further in Neuroglial and Gliovascular Interactions , 2022 .

[80]  Michael Z. Lin,et al.  Genetically encoded indicators of neuronal activity , 2016, Nature Neuroscience.

[81]  Elvire Guiot,et al.  Single‐fluorophore biosensors based on conformation‐sensitive GFP variants , 2014, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[82]  Ian Parker,et al.  A comparison of fluorescent Ca²⁺ indicators for imaging local Ca²⁺ signals in cultured cells. , 2015, Cell calcium.

[83]  J. Lacaille,et al.  Astrocytes Are Endogenous Regulators of Basal Transmission at Central Synapses , 2011, Cell.

[84]  N. Ropert,et al.  Lack of Evidence for Vesicular Glutamate Transporter Expression in Mouse Astrocytes , 2013, The Journal of Neuroscience.

[85]  Edith Hamel,et al.  Brain Perfusion and Astrocytes , 2018, Trends in Neurosciences.

[86]  B. Barres,et al.  Genomic Analysis of Reactive Astrogliosis , 2012, The Journal of Neuroscience.

[87]  Philipp J. Keller,et al.  Whole-brain functional imaging at cellular resolution using light-sheet microscopy , 2013, Nature Methods.

[88]  Stefan R. Pulver,et al.  Genetically encoded calcium indicators for multi-color neural activity imaging and combination with optogenetics , 2013, Front. Mol. Neurosci..

[89]  Miguel Maravall,et al.  The Barrel Cortex as a Model to Study Dynamic Neuroglial Interaction , 2009, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.