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Toll‐like receptor expression in murine DC subsets: lack of TLR7 expression by CD8α<sup>+</sup> DC correlates with unresponsiveness to imidazoquinolines

European Journal of Immunology · 2003 · Vol. 33(4) · pp. 827–833
Alexander D. EdwardsSandra S. DieboldEmma SlackHideyuki TomizawaHiroaki HemmiTsuneyasu KaishoShizuo AkiraCaetano Reis e Sousa

Abstract

Toll-like receptors (TLR) recognize microbial and viral patterns and activate dendritic cells (DC). TLR distribution among human DC subsets is heterogeneous: plasmacytoid DC (PDC) express TLR1, 7 and 9, while other DC types do not express TLR9 but express other TLR. Here, we report that mRNA for most TLR is expressed at similar levels by murine splenic DC sub-types, including PDC, but that TLR3 is preferentially expressed by CD8 alpha(+) DC while TLR5 and TLR7 are selectively absent from the same subset. Consistent with the latter, TLR7 ligand activates CD8 alpha(-) DC and PDC, but not CD8 alpha(+) DC as measured by survival ex vivo, up-regulation of surface markers and production of IL-12p40. These data suggest that the dichotomy in TLR expression between plasmacytoid and non-plasmacytoid DC is not conserved between species. However, lack of TLR7 expression could restrict the involvement of CD8 alpha(+) DC in recognition of certain mouse pathogens.

Immune Response and InflammationImmunotherapy and Immune ResponsesImmune Cell Function and InteractionBiologyTLR7CD8Toll-like receptorImmunologyReceptorExpression (computer science)Cell biologyMolecular biologyImmune system

MeSH terms

AnimalsCells, CulturedDendritic CellsFemaleImidazolesMaleMembrane GlycoproteinsMice, Inbred BALB CMice, Inbred C57BLReceptors, Cell SurfaceRNA, MessengerSpecies SpecificitySpleenTranscription, GeneticCD8 Antigens
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