Identification of a novel mechanism of blood-brain communication during peripheral inflammation via choroid plexus-derived extracellular vesicles

EMBO Mol Med. 2016 Oct 4;8(10):1162-1183. doi: 10.15252/emmm.201606271. Print 2016 Oct.

Abstract

Here, we identified release of extracellular vesicles (EVs) by the choroid plexus epithelium (CPE) as a new mechanism of blood-brain communication. Systemic inflammation induced an increase in EVs and associated pro-inflammatory miRNAs, including miR-146a and miR-155, in the CSF Interestingly, this was associated with an increase in amount of multivesicular bodies (MVBs) and exosomes per MVB in the CPE cells. Additionally, we could mimic this using LPS-stimulated primary CPE cells and choroid plexus explants. These choroid plexus-derived EVs can enter the brain parenchyma and are taken up by astrocytes and microglia, inducing miRNA target repression and inflammatory gene up-regulation. Interestingly, this could be blocked in vivo by intracerebroventricular (icv) injection of an inhibitor of exosome production. Our data show that CPE cells sense and transmit information about the peripheral inflammatory status to the central nervous system (CNS) via the release of EVs into the CSF, which transfer this pro-inflammatory message to recipient brain cells. Additionally, we revealed that blockage of EV secretion decreases brain inflammation, which opens up new avenues to treat systemic inflammatory diseases such as sepsis.

Keywords: blood–brain barrier; choroid plexus; exosomes; extracellular vesicles; sepsis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood-Brain Barrier / pathology*
  • Brain / pathology*
  • Cells, Cultured
  • Cerebrospinal Fluid / chemistry
  • Choroid Plexus / metabolism*
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism
  • Extracellular Vesicles / metabolism*
  • Immunologic Factors / metabolism
  • Inflammation / pathology*
  • Lipopolysaccharides / metabolism
  • Mice, Inbred C57BL
  • MicroRNAs / analysis
  • Organ Culture Techniques

Substances

  • Immunologic Factors
  • Lipopolysaccharides
  • MicroRNAs
  • Mirn146 microRNA, mouse
  • Mirn155 microRNA, mouse