An Antimicrobial Peptide and Its Neuronal Receptor Regulate Dendrite Degeneration in Aging and Infection

Neuron. 2018 Jan 3;97(1):125-138.e5. doi: 10.1016/j.neuron.2017.12.001.

Abstract

Infections have been identified as possible risk factors for aging-related neurodegenerative diseases, but it remains unclear whether infection-related immune molecules have a causative role in neurodegeneration during aging. Here, we reveal an unexpected role of an epidermally expressed antimicrobial peptide, NLP-29 (neuropeptide-like protein 29), in triggering aging-associated dendrite degeneration in C. elegans. The age-dependent increase of nlp-29 expression is regulated by the epidermal tir-1/SARM-pmk-1/p38 MAPK innate immunity pathway. We further identify an orphan G protein-coupled receptor NPR-12 (neuropeptide receptor 12) acting in neurons as a receptor for NLP-29 and demonstrate that the autophagic machinery is involved cell autonomously downstream of NPR-12 to transduce degeneration signals. Finally, we show that fungal infections cause dendrite degeneration using a similar mechanism as in aging, through NLP-29, NPR-12, and autophagy. Our findings reveal an important causative role of antimicrobial peptides, their neuronal receptors, and the autophagy pathway in aging- and infection-associated dendrite degeneration.

Keywords: AMP; G protein-coupled receptor; GPCR; aging; antimicrobial peptide; autophagy; dendrite degeneration; infection.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / immunology
  • Aging / metabolism*
  • Aging / pathology
  • Animals
  • Antimicrobial Cationic Peptides / metabolism*
  • Autophagy / physiology
  • Caenorhabditis elegans
  • Dendrites / metabolism
  • Dendrites / pathology*
  • Mycoses / immunology
  • Mycoses / pathology
  • Nerve Degeneration / immunology
  • Nerve Degeneration / metabolism*
  • Rats
  • Receptors, G-Protein-Coupled / metabolism

Substances

  • Antimicrobial Cationic Peptides
  • Receptors, G-Protein-Coupled