MYO18B promotes lysosomal exocytosis by facilitating focal adhesion maturation

J Cell Biol. 2025 Mar 3;224(3):e202407068. doi: 10.1083/jcb.202407068. Epub 2025 Jan 3.

Abstract

Many cancer cells exhibit increased amounts of paucimannose glycans, which are truncated N-glycan structures rarely found in mammals. Paucimannosidic proteins are proposedly generated within lysosomes and exposed on the cell surface through a yet uncertain mechanism. In this study, we revealed that paucimannosidic proteins are produced by lysosomal glycosidases and secreted via lysosomal exocytosis. Interestingly, lysosomal exocytosis preferentially occurred in the vicinity of focal adhesions, protein complexes connecting the actin cytoskeleton to the extracellular matrix. Through genome-wide knockout screening, we identified that MYO18B, an actin crosslinker, is required for focal adhesion maturation, facilitating lysosomal exocytosis and the release of paucimannosidic lysosomal proteins to the extracellular milieu. Moreover, a mechanosensitive cation channel PIEZO1 locally activated at focal adhesions imports Ca2+ necessary for lysosome-plasma membrane fusion. Collectively, our study unveiled an intimate relationship between lysosomal exocytosis and focal adhesion, shedding light on the unexpected interplay between lysosomal activities and cellular mechanosensing.

MeSH terms

  • Animals
  • Calcium / metabolism
  • Exocytosis*
  • Focal Adhesions* / genetics
  • Focal Adhesions* / metabolism
  • Humans
  • Ion Channels / genetics
  • Ion Channels / metabolism
  • Lysosomes* / metabolism
  • Membrane Fusion
  • Myosins* / genetics
  • Myosins* / metabolism

Substances

  • Myosins
  • Ion Channels
  • PIEZO1 protein, human
  • Calcium