FB2024_03 , released June 25, 2024
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Citation
Ryabova, E.V., Melentev, P.A., Komissarov, A.E., Surina, N.V., Ivanova, E.A., Matiytsiv, N., Shcherbata, H.R., Sarantseva, S.V. (2021). Morpho-Functional Consequences of Swiss Cheese Knockdown in Glia of Drosophila melanogaster.  Cells 10(3): 529.
FlyBase ID
FBrf0248557
Publication Type
Research paper
Abstract
Glia are crucial for the normal development and functioning of the nervous system in many animals. Insects are widely used for studies of glia genetics and physiology. Drosophila melanogaster surface glia (perineurial and subperineurial) form a blood-brain barrier in the central nervous system and blood-nerve barrier in the peripheral nervous system. Under the subperineurial glia layer, in the cortical region of the central nervous system, cortex glia encapsulate neuronal cell bodies, whilst in the peripheral nervous system, wrapping glia ensheath axons of peripheral nerves. Here, we show that the expression of the evolutionarily conserved swiss cheese gene is important in several types of glia. swiss cheese knockdown in subperineurial glia leads to morphological abnormalities of these cells. We found that the number of subperineurial glia nuclei is reduced under swiss cheese knockdown, possibly due to apoptosis. In addition, the downregulation of swiss cheese in wrapping glia causes a loss of its integrity. We reveal transcriptome changes under swiss cheese knockdown in subperineurial glia and in cortex + wrapping glia and show that the downregulation of swiss cheese in these types of glia provokes reactive oxygen species acceleration. These results are accompanied by a decline in animal mobility measured by the negative geotaxis performance assay.
PubMed ID
PubMed Central ID
PMC7998100 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Cells
    Title
    Cells
    ISBN/ISSN
    2073-4409
    Data From Reference
    Alleles (7)
    Genes (3)
    Human Disease Models (1)
    Insertions (5)
    Transgenic Constructs (2)