Neutral sphingomyelinase 2 controls exosome secretion by counteracting V-ATPase-mediated endosome acidification

J Cell Sci. 2022 Mar 1;135(5):jcs259324. doi: 10.1242/jcs.259324. Epub 2022 Feb 28.

Abstract

During endosome maturation, neutral sphingomyelinase 2 (nSMase2, encoded by SMPD3) is involved in budding of intraluminal vesicles (ILVs) into late endosomes or multivesicular bodies (MVBs). Fusion of these with the plasma membrane results in secretion of exosomes or small extracellular vesicles (sEVs). Here, we report that nSMase2 activity controls sEV secretion through modulation of vacuolar H+-ATPase (V-ATPase) activity. Specifically, we show that nSMase2 inhibition induces V-ATPase complex assembly that drives MVB lumen acidification and consequently reduces sEV secretion. Conversely, we further demonstrate that stimulating nSMase2 activity with the inflammatory cytokine TNFα (also known as TNF) decreases acidification and increases sEV secretion. Thus, we find that nSMase2 activity affects MVB membrane lipid composition to counteract V-ATPase-mediated endosome acidification, thereby shifting MVB fate towards sEV secretion. This article has an associated First Person interview with the first author of the paper.

Keywords: Endosomal cargo sorting; Endosomal maturation; Intraluminal vesicles; Secretory multivesicular bodies; Small extracellular vesicles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Endosomal Sorting Complexes Required for Transport / metabolism
  • Endosomes / metabolism
  • Exosomes* / metabolism
  • Humans
  • Hydrogen-Ion Concentration
  • Multivesicular Bodies / metabolism
  • Protein Transport
  • Sphingomyelin Phosphodiesterase / genetics
  • Sphingomyelin Phosphodiesterase / metabolism
  • Vacuolar Proton-Translocating ATPases* / genetics
  • Vacuolar Proton-Translocating ATPases* / metabolism

Substances

  • Endosomal Sorting Complexes Required for Transport
  • Sphingomyelin Phosphodiesterase
  • Vacuolar Proton-Translocating ATPases