Carbon nanotubes, but not spherical nanoparticles, block autophagy by a shape-related targeting of lysosomes in murine macrophages

Autophagy. 2018;14(8):1323-1334. doi: 10.1080/15548627.2018.1474993. Epub 2018 Jul 30.

Abstract

Nanoparticles (NPs) can be toxic, depending on their physico-chemical characteristics. Macroautophagy/autophagy could represent a potential underlying mechanism of this toxicity. We therefore set up a study aimed to characterize in depth the effects, on autophagy, of macrophage exposure to NPs, with a particular attention paid to the role of NP physico-chemical characteristics (specifically chemical composition, shape, size, length, crystal phase, and/or surface properties). We demonstrate that exposure to carbon nanotubes (CNT) but not to spherical NPs leads to the blockage of the autophagic flux. We further identified lysosomal dysfunction, in association with the downregulation of SNAPIN expression, as the underlying mechanism responsible for the CNT-induced autophagy blockade. These results identify for the first time the shape as a major determinant of the interaction of NPs with the autophagy pathway. Moreover, identifying the lysosomes and SNAPIN as primary targets of MWCNT toxicity opens new directions in the interpretation and understanding of nanomaterial toxicity.

Keywords: Autophagy; carbon nanotubes; lysosomes; physico-chemical characteristics; titanium dioxide.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagy* / drug effects
  • Biomarkers / metabolism
  • Endocytosis / drug effects
  • Lysosomal-Associated Membrane Protein 1 / metabolism
  • Lysosomes / drug effects
  • Lysosomes / metabolism*
  • Lysosomes / ultrastructure
  • Macrophages / cytology*
  • Macrophages / drug effects
  • Macrophages / metabolism*
  • Macrophages / ultrastructure
  • Mice
  • Microtubule-Associated Proteins / metabolism
  • Nanoparticles / chemistry
  • Nanoparticles / toxicity*
  • Nanoparticles / ultrastructure
  • Nanotubes, Carbon / chemistry
  • Nanotubes, Carbon / toxicity*
  • Nanotubes, Carbon / ultrastructure
  • RAW 264.7 Cells
  • Titanium / pharmacology
  • Vesicular Transport Proteins / metabolism

Substances

  • Biomarkers
  • Lysosomal-Associated Membrane Protein 1
  • Map1lc3b protein, mouse
  • Microtubule-Associated Proteins
  • Nanotubes, Carbon
  • Snapin protein, mouse
  • Vesicular Transport Proteins
  • titanium dioxide
  • Titanium

Grants and funding

This work was supported by the Agence Nationale de la recherche (ANR) [ANR-13-CESA-0010-01]; LabEx SERENADE [11-LABX-0064].