iScience (Apr 2024)

Cell non-autonomous control of autophagy and metabolism by glial cells

  • Melissa G. Metcalf,
  • Samira Monshietehadi,
  • Arushi Sahay,
  • Jenni Durieux,
  • Ashley E. Frakes,
  • Martina Velichkovska,
  • Cesar Mena,
  • Amelia Farinas,
  • Melissa Sanchez,
  • Andrew Dillin

Journal volume & issue
Vol. 27, no. 4
p. 109354

Abstract

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Summary: Glia are the protectors of the nervous system, providing neurons with support and protection from cytotoxic insults. We previously discovered that four astrocyte-like glia can regulate organismal proteostasis and longevity in C. elegans. Expression of the UPRER transcription factor, XBP-1s, in these glia increases stress resistance, and longevity, and activates the UPRER in intestinal cells via neuropeptides. Autophagy, a key regulator of metabolism and aging, has been described as a cell autonomous process. Surprisingly, we find that glial XBP-1s enhances proteostasis and longevity by cell non-autonomously reprogramming organismal lipid metabolism and activating autophagy. Glial XBP-1s regulates the activation of another transcription factor, HLH-30/TFEB, in the intestine. HLH-30 activates intestinal autophagy, increases intestinal lipid catabolism, and upregulates a robust transcriptional program. Our study reveals a novel role for glia in regulating peripheral lipid metabolism, autophagy, and organellar health through peripheral activation of HLH-30 and autophagy.

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