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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