| Literature DB >> 25762685 |
Anne-Cécile Boulay1, Aurélien Mazeraud2, Salvatore Cisternino3, Bruno Saubaméa3, Phillipe Mailly1, Laurent Jourdren4, Corinne Blugeon4, Virginie Mignon3, Maria Smirnova3, Alessia Cavallo1, Pascal Ezan1, Patrick Avé2, Florent Dingli5, Damarys Loew5, Paulo Vieira6, Fabrice Chrétien2, Martine Cohen-Salmon7.
Abstract
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.Entities:
Keywords: astrocyte; autoimmunity; blood-brain barrier; connexin; immune quiescence
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Year: 2015 PMID: 25762685 PMCID: PMC6605289 DOI: 10.1523/JNEUROSCI.2575-14.2015
Source DB: PubMed Journal: J Neurosci ISSN: 0270-6474 Impact factor: 6.167