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.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.