Geijtenbeek Teunis B H, Engering Anneke, Van Kooyk Yvette
Department of Molecular Cell Biology, Vrije Universiteit Medical Center Amsterdam, The Netherlands.
J Leukoc Biol. 2002 Jun;71(6):921-31.
Dendritic cells (DC) are present in essentially every tissue where they operate at the interface of innate and acquired immunity by recognizing pathogens and presenting pathogen-derived peptides to T cells. It is becoming clear that not all C-type lectins on DC serve as antigen receptors recognizing pathogens through carbohydrate structures. The C-type lectin DC-SIGN is unique in that it regulates adhesion processes, such as DC trafficking and T-cell synapse formation, as well as antigen capture. Moreover, even though several C-type lectins have been shown to bind HIV-1, DC-SIGN does not only capture HIV-1 but also protects it in early endosomes allowing HIV-1 transport by DC to lymphoid tissues, where it enhances trans infection of T cells. Here we discuss the carbohydrate/protein recognition profile and other features of DC-SIGN that contribute to the potency of DC to control immunity.
树突状细胞(DC)几乎存在于每一种组织中,它们通过识别病原体并将病原体衍生的肽呈递给T细胞,在固有免疫和获得性免疫的界面发挥作用。越来越清楚的是,并非DC上所有的C型凝集素都作为通过碳水化合物结构识别病原体的抗原受体。C型凝集素DC-SIGN的独特之处在于,它不仅调节诸如DC迁移和T细胞突触形成等黏附过程,还调节抗原捕获。此外,尽管已经证明几种C型凝集素能结合HIV-1,但DC-SIGN不仅能捕获HIV-1,还能在早期内体中保护它,使HIV-1能够由DC转运至淋巴组织,在那里增强对T细胞的转染。在此,我们讨论DC-SIGN的碳水化合物/蛋白质识别特征以及其他有助于DC控制免疫能力的特征。