| Literature DB >> 17082582 |
Rodrigo Pacheco1, Harold Oliva, José M Martinez-Navío, Núria Climent, Francisco Ciruela, José M Gatell, Teresa Gallart, Josefa Mallol, Carmen Lluis, Rafael Franco.
Abstract
Adaptive immune responses begin after productive immunosynaptic contacts formation established in secondary lymphoid organs by dendritic cells (DC) presenting the Ag to T lymphocytes. Despite its resemblance to the neurosynapse, the participation of soluble small nonpeptidic mediators in the intercellular cross-talk taking place during T cell-DC interactions remains poorly studied. In this study, we show that human DC undergoing maturation and in contact with T cells release significant amounts of glutamate, which is the main excitatory neurotransmitter in mammalians. The release of glutamate is nonvesicular and mediated by the DC-expressed Xc- cystine/glutamate antiporter. DC-derived glutamate stimulating the constitutively expressed metabotropic glutamate receptor 5 impairs T cell activation. However, after productive Ag presentation, metabotropic glutamate receptor 1 is expressed in T cells to mediate enhanced T cell proliferation and secretion of Th1 and proinflammatory cytokines. These data suggest that, during T cell-DC interaction, glutamate is a novel and highly effective regulator in the initiation of T cell-mediated immune responses.Entities:
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Year: 2006 PMID: 17082582 DOI: 10.4049/jimmunol.177.10.6695
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422