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    The astrocyte network in the ventral nerve cord neuropil of the Drosophila third-instar larva

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    Author
    Hernandez, Ernesto
    MacNamee, Sarah E
    Kaplan, Leah R
    Lance, Kim
    Garcia-Verdugo, Hector D
    Farhadi, Dara S
    Deer, Christine
    Lee, Si W
    Oland, Lynne A
    Affiliation
    Univ Arizona, Dept Neurosci
    Univ Arizona, Coll Med
    Univ Arizona, Univ Informat Technol Serv, Data Visualizat Team, Res Technol Grp
    Issue Date
    2020-01-07
    Keywords
    glial cells
    neuron-glia interaction
    RRID; BDSC Cat# 30125
    RRID; BDSC Cat# 4775
    RRID; BDSC Cat# 6938
    RRID; BDSC Cat# 64085
    RRID; BDSC Cat# 5692
    RRID; BDSC Cat# 38760
    RRID; Molecular Probes Cat# 6455
    RRID; Jackson ImmunoResearch Labs Cat# 115-167-003
    RRID; Molecular Probes Cat# A-21236
    RRID; Bio-rad Cat # MCA1360
    RRID; Cell Signaling Technology Cat # 3724
    RRID; Novus Cat # NBP1-06712
    RRID; Abcam Cat# ab6953
    RRID; DSHB Cat# nc82
    RRID; Thermo Fisher Scientific Cat# A-11034
    RRID:AB_2576217
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    Publisher
    WILEY
    Citation
    Hernandez, E, MacNamee, SE, Kaplan, LR, et al. The astrocyte network in the ventral nerve cord neuropil of the Drosophila third‐instar larva. J Comp Neurol. 2020; 1– 21. https://doi.org/10.1002/cne.24852
    Journal
    JOURNAL OF COMPARATIVE NEUROLOGY
    Rights
    © 2020 Wiley Periodicals, Inc.
    Collection Information
    This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
    Abstract
    Understanding neuronal function at the local and circuit level requires understanding astrocyte function. We have provided a detailed analysis of astrocyte morphology and territory in the Drosophila third-instar ventral nerve cord where there already exists considerable understanding of the neuronal network. Astrocyte shape varies more than previously reported; many have bilaterally symmetrical partners, many have a high percentage of their arborization in adjacent segments, and many have branches that follow structural features. Taken together, our data are consistent with, but not fully explained by, a model of a developmental growth process dominated by competitive or repulsive interactions between astrocytes. Our data suggest that the model should also include cell-autonomous aspects, as well as the use of structural features for growth. Variation in location of arborization territory for identified astrocytes was great enough that a standardized scheme of neuropil division among the six astrocytes that populate each hemi-segment is not possible at the third instar. The arborizations of the astrocytes can extend across neuronal functional domains. The ventral astrocyte in particular, whose territory can extend well into the proprioceptive region of the neuropil, has no obvious branching pattern that correlates with domains of particular sensory modalities, suggesting that the astrocyte would respond to neuronal activity in any of the sensory modalities, perhaps integrating across them. This study sets the stage for future studies that will generate a robust, functionally oriented connectome that includes both partners in neuronal circuits-the neurons and the glial cells, providing the foundation necessary for studies to elucidate neuron-glia interactions in this neuropil.
    Note
    12 month embargo; published online: 7 January 2020
    ISSN
    0021-9967
    EISSN
    1096-9861
    PubMed ID
    31909826
    DOI
    10.1002/cne.24852
    Version
    Final accepted manuscript
    Sponsors
    NSF, Division of Integrative Organismal SystemsNational Science Foundation (NSF) [IOS1353739]; State of Arizona: University of Arizona
    ae974a485f413a2113503eed53cd6c53
    10.1002/cne.24852
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