Fcγ Receptor–mediated Induction of Dendritic Cell Maturation and Major Histocompatibility Complex Class I–restricted Antigen Presentation after Immune Complex Internalization

Armelle Régnault(Chiba University), Danielle Lankar(Inserm), Valérie Lacabanne(Inserm), Ana Rodrı́guez(Inserm), Clotilde Théry(Inserm), María Rescigno(Chiba University), Takashi Saito(Chiba University), Sjef Verbeek(Chiba University), Christian Bonnerot(Inserm), Paola Ricciardi‐Castagnoli(Chiba University), Sebastián Amigorena(Chiba University)
The Journal of Experimental Medicine
January 18, 1999
Cited by 882Open Access
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Abstract

Dendritic cells (DCs) express several receptors for the Fc portion of immunoglobulin (Ig)G (FcgammaR), which mediate internalization of antigen-IgG complexes (immune complexes, ICs) and promote efficient major histocompatibility complex (MHC) class II-restricted antigen presentation. We now show that FcgammaRs have two additional specific attributes in murine DCs: the induction of DC maturation and the promotion of efficient MHC class I-restricted presentation of peptides from exogenous, IgG-complexed antigens. Both FcgammaR functions require the FcgammaR-associated gamma chain. FcgammaR-mediated MHC class I-restricted antigen presentation is extremely sensitive and specific to immature DCs. It requires proteasomal degradation and is dependent on functional peptide transporter associated with antigen processing, TAP1-TAP2. By promoting DC maturation and presentation on both MHC class I and II molecules, ICs should efficiently sensitize DCs for priming of both CD4(+) helper and CD8(+) cytotoxic T lymphocytes in vivo.


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