Dual microglia effects on blood brain barrier permeability induced by systemic inflammation

Nat Commun. 2019 Dec 20;10(1):5816. doi: 10.1038/s41467-019-13812-z.

Abstract

Microglia survey brain parenchyma, responding to injury and infections. Microglia also respond to systemic disease, but the role of blood-brain barrier (BBB) integrity in this process remains unclear. Using simultaneous in vivo imaging, we demonstrated that systemic inflammation induces CCR5-dependent migration of brain resident microglia to the cerebral vasculature. Vessel-associated microglia initially maintain BBB integrity via expression of the tight-junction protein Claudin-5 and make physical contact with endothelial cells. During sustained inflammation, microglia phagocytose astrocytic end-feet and impair BBB function. Our results show microglia play a dual role in maintaining BBB integrity with implications for elucidating how systemic immune-activation impacts neural functions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Astrocytes / immunology
  • Astrocytes / metabolism
  • Blood-Brain Barrier / diagnostic imaging
  • Blood-Brain Barrier / immunology
  • Blood-Brain Barrier / metabolism*
  • Cerebrovascular Circulation / immunology*
  • Claudin-5 / immunology
  • Claudin-5 / metabolism
  • Disease Models, Animal
  • Endothelial Cells / immunology
  • Endothelial Cells / metabolism*
  • Humans
  • Intravital Microscopy
  • Lupus Erythematosus, Systemic / immunology*
  • Male
  • Mice
  • Microglia / immunology*
  • Microglia / metabolism
  • Permeability
  • Phagocytosis / immunology
  • Receptors, CCR5 / immunology
  • Receptors, CCR5 / metabolism
  • Stereotaxic Techniques
  • Tight Junctions / immunology
  • Tight Junctions / metabolism

Substances

  • CCR5 protein, mouse
  • Claudin-5
  • Cldn5 protein, mouse
  • Receptors, CCR5