FB2024_03 , released June 25, 2024
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Citation
Zhang, F., Zhao, Y., Chao, Y., Muir, K., Han, Z. (2013). Cubilin and amnionless mediate protein reabsorption in Drosophila nephrocytes.  J. Am. Soc. Nephrol. 24(2): 209--216.
FlyBase ID
FBrf0220701
Publication Type
Research paper
Abstract
The insect nephrocyte and the mammalian glomerular podocyte are similar with regard to filtration, but it remains unclear whether there is an organ or cell type in flies that reabsorbs proteins. Here, we show that the Drosophila nephrocyte has molecular, structural, and functional similarities to the renal proximal tubule cell. We screened for genes required for nephrocyte function and identified two Drosophila genes encoding orthologs of mammalian cubilin and amnionless (AMN), two major receptors for protein reabsorption in the proximal tubule. In Drosophila, expression of dCubilin and dAMN is specific to nephrocytes, where they function as co-receptors for protein uptake. Targeted expression of human AMN in Drosophila nephrocytes was sufficient to rescue defective protein uptake induced by dAMN knockdown, suggesting evolutionary conservation of Cubilin/AMN co-receptors function from flies to humans. Furthermore, we found that Cubilin/AMN-mediated protein reabsorption is required for the maintenance of nephrocyte ultrastructure and fly survival under conditions of toxic stress. In conclusion, the insect nephrocyte combines filtration with protein reabsorption, using evolutionarily conserved genes and subcellular structures, suggesting that it can serve as a simplified model for both podocytes and the renal proximal tubule.
PubMed ID
PubMed Central ID
PMC3559489 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    J. Am. Soc. Nephrol.
    Title
    Journal of the American Society of Nephrology
    Publication Year
    1990-
    ISBN/ISSN
    1046-6673
    Data From Reference
    Alleles (7)
    Genes (6)
    Human Disease Models (2)
    Natural transposons (1)
    Experimental Tools (2)
    Transgenic Constructs (7)