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Immune quiescence of the brain is set by astroglial connexin 43.

Anne-Cécile BoulayAurélien MazeraudSalvatore CisterninoBruno SaubaméaPhillipe MaillyLaurent JourdrenCorinne BlugeonVirginie MignonMaria SmirnovaAlessia CavalloPascal EzanPatrick AvéFlorent DingliDamarys LoewPaulo VieiraFabrice ChrétienMartine Cohen Salmon
Published in: The Journal of neuroscience : the official journal of the Society for Neuroscience (2015)
In the normal brain, immune cell trafficking and immune responses are strictly controlled and limited. This unique homeostatic equilibrium, also called brain immune quiescence, is crucial to maintaining proper brain functions and is altered in various pathological processes, from chronic immunopathological disorders to cognitive and psychiatric impairments. To date, the precise nature of factors regulating the brain/immune system interrelationship is poorly understood. In the present study, we demonstrate that one of these regulating factors is Connexin 43 (Cx43), a gap junction protein highly expressed by astrocytes at the blood-brain barrier (BBB) interface. We show that, by setting the activated state of cerebral endothelium, astroglial Cx43 controls immune recruitment as well as antigen presentation mechanisms in the mouse brain. Consequently, in the absence of astroglial Cx43, recruited immune cells elaborate a specific humoral autoimmune response against the von Willebrand factor A domain-containing protein 5a, an extracellular matrix protein of the brain. Altogether, our results demonstrate that Cx43 is a new astroglial factor promoting the immune quiescence of the brain.
Keyphrases
  • resting state
  • white matter
  • immune response
  • functional connectivity
  • cerebral ischemia
  • multiple sclerosis
  • dendritic cells
  • binding protein