FB2026_02 , released June 18, 2026
FB2026_02 , released June 18, 2026
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Citation
Campos-Blázquez, J.P., Schuth, N., Garay, E., Clark, A.H., Vogelsang, U., Nachtegaal, M., Contreras, R.G., Quintanar, L., Missirlis, F. (2022). Chloroquine disrupts zinc storage granules in primary Malpighian tubule cells of Drosophila melanogaster.  Metallomics 14(10): mfac075.
FlyBase ID
FBrf0254673
Publication Type
Research paper
Abstract
Contrasting reports exist in the literature regarding the effect of chloroquine treatment on cellular zinc uptake or secretion. Here, we tested the effect of chloroquine administration in the Drosophila model organism. We show that larvae grown on a diet supplemented with 2.5 mg/ml chloroquine lose up to 50% of their stored zinc and around 10% of their total potassium content. This defect in chloroquine-treated animals correlates with the appearance of abnormal autophagolysosomes in the principal cells of the Malpighian tubules, where zinc storage granules reside. We further show that the reported increase of Fluozin-3 fluorescence following treatment of cells with 300 μM chloroquine for 1 h may not reflect increased zinc accumulation, since a similar treatment in Madin-Darby canine kidney cells results in a 36% decrease in their total zinc content. Thus, chloroquine should not be considered a zinc ionophore. Zinc supplementation plus chloroquine treatment restored zinc content both in vivo and in vitro, without correcting autophagic or other ionic alterations, notably in potassium, associated with the chloroquine treatment. We suggest that chloroquine or hydroxychloroquine administration to patients could reduce intracellular zinc storage pools and be part of the drug's mechanism of action.
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    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Metallomics
    Title
    Metallomics : integrated biometal science
    ISBN/ISSN
    1756-5901 1756-591X
    Data From Reference
    Chemicals (1)
    Genes (1)
    Human Disease Models (1)