| Literature DB >> 29175168 |
Hadi Zarif1, Sarah Nicolas1, Mélanie Guyot2, Salma Hosseiny1, Anne Lazzari2, María Magdalena Canali2, Julie Cazareth1, Frédéric Brau1, Valentine Golzné1, Elisa Dourneau1, Maud Maillaut1, Carmelo Luci3, Agnès Paquet1, Kevin Lebrigand1, Marie-Jeanne Arguel1, Douglas Daoudlarian2, Catherine Heurteaux1, Nicolas Glaichenhaus2, Joëlle Chabry4, Alice Guyon5, Agnès Petit-Paitel1.
Abstract
Enriched environment (EE) induces plasticity changes in the brain. Recently, CD4+ T cells have been shown to be involved in brain plasticity processes. Here, we show that CD8+ T cells are required for EE-induced brain plasticity in mice, as revealed by measurements of hippocampal volume, neurogenesis in the DG of the hippocampus, spinogenesis and glutamatergic synaptic function in the CA of the hippocampus. As a consequence, EE-induced behavioral benefits depend, at least in part, on CD8+ T cells. In addition, we show that spleen CD8+ T cells from mice housed in standard environment (SE) and EE have different properties in terms of 1) TNFα release after in vitro CD3/CD28 or PMA/Iono stimulation 2) in vitro proliferation properties 3) CD8+ CD44+ CD62Llow and CD62Lhi T cells repartition 4) transcriptomic signature as revealed by RNA sequencing. CD8+ T cells purified from the choroid plexus of SE and EE mice also exhibit different transcriptomic profiles as highlighted by single-cell mRNA sequencing. We show that CD8+ T cells are essential mediators of beneficial EE effects on brain plasticity and cognition. Additionally, we propose that EE differentially primes CD8+ T cells leading to behavioral improvement.Entities:
Keywords: Behavior; Brain plasticity; CD8(+) T cells; Choroid plexus; Enriched environment; Hippocampus; Long term potentiation; Mice; Neurogenesis; Synaptogenesis
Mesh:
Year: 2017 PMID: 29175168 DOI: 10.1016/j.bbi.2017.11.016
Source DB: PubMed Journal: Brain Behav Immun ISSN: 0889-1591 Impact factor: 7.217