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Identification of a novel anoikis signalling pathway using the fungal virulence factor gliotoxin

Author

Listed:
  • Florian Haun

    (Albert Ludwigs University Freiburg
    Albert Ludwigs University Freiburg
    Albert Ludwigs University Freiburg)

  • Simon Neumann

    (Albert Ludwigs University Freiburg)

  • Lukas Peintner

    (Albert Ludwigs University Freiburg)

  • Katrin Wieland

    (Albert Ludwigs University Freiburg)

  • Jüri Habicht

    (University Hospital Heidelberg)

  • Carsten Schwan

    (Albert Ludwigs University Freiburg)

  • Kristine Østevold

    (Albert Ludwigs University Freiburg)

  • Maria Magdalena Koczorowska

    (Albert Ludwigs University Freiburg)

  • Martin Biniossek

    (Albert Ludwigs University Freiburg)

  • Matthias Kist

    (Albert Ludwigs University Freiburg)

  • Hauke Busch

    (Albert Ludwigs University Freiburg
    University of Lübeck)

  • Melanie Boerries

    (Albert Ludwigs University Freiburg
    German Cancer Research Center (DKFZ))

  • Roger J. Davis

    (University of Massachusetts Medical School)

  • Ulrich Maurer

    (Albert Ludwigs University Freiburg
    Albert Ludwigs University Freiburg
    BIOSS Centre for Biological Signalling Studies)

  • Oliver Schilling

    (Albert Ludwigs University Freiburg
    Albert Ludwigs University Freiburg
    BIOSS Centre for Biological Signalling Studies)

  • Klaus Aktories

    (Albert Ludwigs University Freiburg
    Albert Ludwigs University Freiburg
    BIOSS Centre for Biological Signalling Studies)

  • Christoph Borner

    (Albert Ludwigs University Freiburg
    Albert Ludwigs University Freiburg
    BIOSS Centre for Biological Signalling Studies)

Abstract

Anoikis is a form of apoptosis induced by cell detachment. Integrin inactivation plays a major role in the process but the exact signalling pathway is ill-defined. Here we identify an anoikis pathway using gliotoxin (GT), a virulence factor of the fungus Aspergillus fumigatus, which causes invasive aspergillosis in humans. GT prevents integrin binding to RGD-containing extracellular matrix components by covalently modifying cysteines in the binding pocket. As a consequence, focal adhesion kinase (FAK) is inhibited resulting in dephosphorylation of p190RhoGAP, allowing activation of RhoA. Sequential activation of ROCK, MKK4/MKK7 and JNK then triggers pro-apoptotic phosphorylation of Bim. Cells in suspension or lacking integrin surface expression are insensitive to GT but are sensitised to ROCK-MKK4/MKK7-JNK-dependent anoikis upon attachment to fibronectin or integrin upregulation. The same signalling pathway is triggered by FAK inhibition or inhibiting integrin αV/β3 with Cilengitide. Thus, GT can target integrins to induce anoikis on lung epithelial cells.

Suggested Citation

  • Florian Haun & Simon Neumann & Lukas Peintner & Katrin Wieland & Jüri Habicht & Carsten Schwan & Kristine Østevold & Maria Magdalena Koczorowska & Martin Biniossek & Matthias Kist & Hauke Busch & Mela, 2018. "Identification of a novel anoikis signalling pathway using the fungal virulence factor gliotoxin," Nature Communications, Nature, vol. 9(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-05850-w
    DOI: 10.1038/s41467-018-05850-w
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    Cited by:

    1. Zili Song & Shuang Zhou & Hongjiao Zhang & Nancy P. Keller & Berl R. Oakley & Xiao Liu & Wen-Bing Yin, 2023. "Fungal secondary metabolism is governed by an RNA-binding protein CsdA/RsdA complex," Nature Communications, Nature, vol. 14(1), pages 1-16, December.

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