Inducin Triggers LC3‐Lipidation and ESCRT‐Mediated Lysosomal Membrane Repair

Author:

Corkery Dale1ORCID,Ursu Andrei2,Lucas Belén2,Grigalunas Michael2ORCID,Kriegler Simon3,Oliva Rosario34ORCID,Dec Robert3,Koska Sandra2,Pahl Axel2ORCID,Sievers Sonja2ORCID,Ziegler Slava2ORCID,Winter Roland3,Wu Yao‐Wen1ORCID,Waldmann Herbert25ORCID

Affiliation:

1. Department of Chemistry Umeå University Umeå Centre for Microbial Research Umeå SE-90187 Sweden

2. Department of Chemical Biology Max Planck Institute of Molecular Physiology Otto-Hahn-Strasse 11 44227 Dortmund Germany

3. Physical Chemistry I – Biophysical Chemistry Department of Chemistry and Chemical Biology TU Dortmund University Otto-Hahn-Strasse 4a, 44227 Dortmund, Germany

4. Present address: Department of Chemical Sciences University of Naples Federico II Via Cintia 4 Naples 80126 Italy

5. Faculty of Chemistry and Chemical Biology Technical University Dortmund Otto-Hahn-Strasse 6 Dortmund 44227 Germany

Abstract

AbstractLipidation of the LC3 protein has frequently been employed as a marker of autophagy. However, LC3‐lipidation is also triggered by stimuli not related to canonical autophagy. Therefore, characterization of the driving parameters for LC3 lipidation is crucial to understanding the biological roles of LC3. We identified a pseudo‐natural product, termed Inducin, that increases LC3 lipidation independently of canonical autophagy, impairs lysosomal function and rapidly recruits Galectin 3 to lysosomes. Inducin treatment promotes Endosomal Sorting Complex Required for Transport (ESCRT)‐dependent membrane repair and transcription factor EB (TFEB)‐dependent lysosome biogenesis ultimately leading to cell death.

Funder

Max-Planck-Gesellschaft

Knut och Alice Wallenbergs Stiftelse

European Commission

Innovative Medicines Initiative

European Federation of Pharmaceutical Industries and Associations

Publisher

Wiley

Subject

Organic Chemistry,Molecular Biology,Molecular Medicine,Biochemistry

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