ADAM17-triggered TNF signalling protects the ageing Drosophila retina from lipid droplet-mediated degeneration

EMBO J. 2020 Sep 1;39(17):e104415. doi: 10.15252/embj.2020104415. Epub 2020 Jul 26.

Abstract

Animals have evolved multiple mechanisms to protect themselves from the cumulative effects of age-related cellular damage. Here, we reveal an unexpected link between the TNF (tumour necrosis factor) inflammatory pathway, triggered by the metalloprotease ADAM17/TACE, and a lipid droplet (LD)-mediated mechanism of protecting retinal cells from age-related degeneration. Loss of ADAM17, TNF and the TNF receptor Grindelwald in pigmented glial cells of the Drosophila retina leads to age-related degeneration of both glia and neurons, preceded by an abnormal accumulation of glial LDs. We show that the glial LDs initially buffer the cells against damage caused by glial and neuronally generated reactive oxygen species (ROS), but that in later life the LDs dissipate, leading to the release of toxic peroxidated lipids. Finally, we demonstrate the existence of a conserved pathway in human iPS-derived microglia-like cells, which are central players in neurodegeneration. Overall, we have discovered a pathway mediated by TNF signalling acting not as a trigger of inflammation, but as a cytoprotective factor in the retina.

Keywords: ADAM17; Glia; lipid droplet; neurodegeneration; reactive oxygen species.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADAM17 Protein / genetics
  • ADAM17 Protein / metabolism*
  • Animals
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism*
  • Drosophila melanogaster
  • Humans
  • Lipid Droplets / metabolism*
  • Lipid Droplets / pathology
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Neuroglia / metabolism*
  • Neuroglia / pathology
  • Reactive Oxygen Species / metabolism
  • Retina / metabolism*
  • Retina / pathology
  • Signal Transduction*
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism*

Substances

  • Drosophila Proteins
  • Membrane Proteins
  • Reactive Oxygen Species
  • Tumor Necrosis Factor-alpha
  • grnd protein, Drosophila
  • ADAM17 Protein