抗原呈递
抗原处理
主要组织相容性复合体
MHC I级
MHC II级
细胞毒性T细胞
生物
抗原
交叉展示
CD8型
免疫学
内化
与抗原处理相关的转运体
启动(农业)
抗原提呈细胞
免疫系统
细胞生物学
树突状细胞
MHC限制
T细胞
受体
生物化学
体外
发芽
植物
作者
Armelle Régnault,Danielle Lankar,Valérie Lacabanne,Ana Rodrı́guez,Clotilde Théry,María Rescigno,Takashi Saito,Sjef Verbeek,Christian Bonnerot,Paola Ricciardi‐Castagnoli,Sebastián Amigorena
标识
DOI:10.1084/jem.189.2.371
摘要
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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