FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Citation
Pogodalla, N., Kranenburg, H., Rey, S., Rodrigues, S., Cardona, A., Klämbt, C. (2021). Drosophila ßHeavy-Spectrin is required in polarized ensheathing glia that form a diffusion-barrier around the neuropil.  Nat. Commun. 12(1): 6357.
FlyBase ID
FBrf0251788
Publication Type
Research paper
Abstract
In the central nervous system (CNS), functional tasks are often allocated to distinct compartments. This is also evident in the Drosophila CNS where synapses and dendrites are clustered in distinct neuropil regions. The neuropil is separated from neuronal cell bodies by ensheathing glia, which as we show using dye injection experiments, contribute to the formation of an internal diffusion barrier. We find that ensheathing glia are polarized with a basolateral plasma membrane rich in phosphatidylinositol-(3,4,5)-triphosphate (PIP3) and the Na+/K+-ATPase Nervana2 (Nrv2) that abuts an extracellular matrix formed at neuropil-cortex interface. The apical plasma membrane is facing the neuropil and is rich in phosphatidylinositol-(4,5)-bisphosphate (PIP2) that is supported by a sub-membranous ßHeavy-Spectrin cytoskeleton. ßHeavy-spectrin mutant larvae affect ensheathing glial cell polarity with delocalized PIP2 and Nrv2 and exhibit an abnormal locomotion which is similarly shown by ensheathing glia ablated larvae. Thus, polarized glia compartmentalizes the brain and is essential for proper nervous system function.
PubMed ID
PubMed Central ID
PMC8569210 (PMC) (EuropePMC)
Related Publication(s)
Erratum

Author Correction: Drosophila ßHeavy-Spectrin is required in polarized ensheathing glia that form a diffusion-barrier around the neuropil.
Pogodalla et al., 2022, Nat. Commun. 13(1): 696 [FBrf0252602]

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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Nat. Commun.
    Title
    Nature communications
    ISBN/ISSN
    2041-1723
    Data From Reference
    Aberrations (1)
    Alleles (25)
    Split System Combinations (1)
    Genes (18)
    Sequence Features (1)
    Natural transposons (1)
    Insertions (10)
    Experimental Tools (2)
    Transgenic Constructs (15)
    Transcripts (8)