Niclosamide Triggers Non-Canonical LC3 Lipidation

Cells. 2019 Mar 15;8(3):248. doi: 10.3390/cells8030248.

Abstract

Autophagy is a highly- evolutionarily-conserved catabolic pathway activated by various cellular stresses. Recently, non-canonical autophagy (NCA), which does not require all of the ATG proteins to form autophagosome or autophagosome-like structures, has been found in various conditions. Moreover, mounting evidence has indicated that non-canonical LC3 lipidation (NCLL) may reflect NCA. We and others have reported that niclosamide (Nic), an anti-helminthic drug approved by the Food and Drug Administration, could induce canonical autophagy via a feedback downregulation of mTOR complex 1. In this study, we found that Nic could also induce NCLL, which is independent of the ULK1 complex and Beclin 1 complex, but dependent on ubiquitin-like conjugation systems. Although bafilomycin A1 and concanamycin A, two known V-ATPase inhibitors, significantly inhibited Nic-induced NCLL, Nic-induced NCLL was demonstrated to be independent of V-ATPase. In addition, the Golgi complex and vimentin were involved in Nic-induced NCLL, which might be a platform or membrane source for Nic-induced LC3-positive structures. These results would be helpful to broaden our understanding of the working mechanisms of Nic and evaluate its pharmacological activities in diseases.

Keywords: Golgi complex; autophagy; bafilomycin A1; niclosamide; non-canonical LC3 lipidation; vimentin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagy-Related Protein-1 Homolog / metabolism
  • Beclin-1 / metabolism
  • Calcium / metabolism
  • Embryo, Mammalian / cytology
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism
  • Golgi Apparatus / drug effects
  • Golgi Apparatus / metabolism
  • HeLa Cells
  • Humans
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Lipids / chemistry*
  • Macrolides / pharmacology
  • Mice
  • Microtubule-Associated Proteins / metabolism*
  • Niclosamide / pharmacology*
  • Ubiquitin / metabolism
  • Vacuolar Proton-Translocating ATPases / metabolism
  • Vimentin / metabolism

Substances

  • Beclin-1
  • Intracellular Signaling Peptides and Proteins
  • Lipids
  • Macrolides
  • Map1lc3b protein, mouse
  • Microtubule-Associated Proteins
  • Ubiquitin
  • Vimentin
  • bafilomycin A1
  • Niclosamide
  • Autophagy-Related Protein-1 Homolog
  • ULK1 protein, human
  • Vacuolar Proton-Translocating ATPases
  • Calcium