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The slit diaphragm in Drosophila exhibits a bilayered, fishnet architecture

Author

Listed:
  • Deborah Moser

    (Goethe University Frankfurt)

  • Konrad Lang

    (Faculty of Medicine and Medical Center - University of Freiburg)

  • Alexandra N. Birtasu

    (Goethe University Frankfurt)

  • Florian Grahammer

    (Martinistraße
    University Medical Center Hamburg-Eppendorf)

  • Martin Helmstädter

    (Faculty of Medicine and Medical Center - University of Freiburg
    Medical Center - University of Freiburg)

  • Margot P. Scheffer

    (Goethe University Frankfurt)

  • Tobias Hermle

    (Faculty of Medicine and Medical Center - University of Freiburg)

  • Achilleas S. Frangakis

    (Goethe University Frankfurt)

Abstract

The kidney relies on the glomerulus to filter large volumes of blood plasma, with the slit diaphragm (SD) as a key structural component of the glomerular filtration barrier. Despite its central role, the molecular architecture of the SD has remained elusive for decades. Using cryo-electron tomography on focused ion beam-milled Drosophila nephrocytes, an invertebrate podocyte model, we show that the SD exhibits a bilayered fishnet architecture. In the cryo-electron tomography map, we observe criss-crossing strands spanning the extracellular space that can be populated with Sns and Kirre, the Drosophila orthologs of nephrin and Neph1, respectively. We show that sns silencing shortens the SD lines until disappearance, linking the fishnet architecture directly to Sns. After Rab5 silencing, which causes Sns mistrafficking and ectopic formation of the SD, the fishnet pattern also appears ectopically. Elucidating the molecular SD architecture establishes a crucial link between the SD organization and its (patho)physiology.

Suggested Citation

  • Deborah Moser & Konrad Lang & Alexandra N. Birtasu & Florian Grahammer & Martin Helmstädter & Margot P. Scheffer & Tobias Hermle & Achilleas S. Frangakis, 2025. "The slit diaphragm in Drosophila exhibits a bilayered, fishnet architecture," Nature Communications, Nature, vol. 16(1), pages 1-10, December.
    • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-64347-5
    DOI: 10.1038/s41467-025-64347-5
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