Autophagic degradation of claudin-5 mediated by its binding to a Clostridium perfringens enterotoxin fragment modulates endothelial barrier permeability

FEBS Lett. 2022 Apr;596(7):924-937. doi: 10.1002/1873-3468.14315. Epub 2022 Feb 21.

Abstract

The blood-brain barrier (BBB) protects the central nervous system (CNS) from harmful elements, while it also restricts efficient drug delivery into the CNS. Previously, we generated a mutated fragment of Clostridium perfringens enterotoxin (cCPEYWSH ) which specifically binds to the endothelial tight junction protein claudin-5. Here, we explore the mechanisms regulating the dynamics of membranous claudin-5 and BBB permeability. Following cCPEYWSH binding to claudin-5, caveolin-1 mediates the redistribution of claudin-5 to the cytosol. This abnormal cytosolic aggregation triggers the autophagic degradation of claudin-5, leading to an increase in BBB permeability. Enhancement or inhibition of autophagy accelerates or inhibits the degradation of cytosolic claudin-5, respectively. Our findings may pave the way for improving BBB permeability for drug delivery.

Keywords: Clostridium perfringens enterotoxin; autophagy; blood-brain barrier; claudin-5; endothelial permeability.

MeSH terms

  • Autophagy
  • Blood-Brain Barrier / metabolism
  • Claudin-5*
  • Clostridium perfringens
  • Enterotoxins* / metabolism
  • Permeability
  • Tight Junctions* / metabolism

Substances

  • Claudin-5
  • Enterotoxins
  • enterotoxin, Clostridium