Blasius Amanda L, Colonna Marco
Department of Pathology and Immunology, Washington University School of Medicine, St Louis, MO 63110, USA.
Trends Immunol. 2006 Jun;27(6):255-60. doi: 10.1016/j.it.2006.04.005. Epub 2006 May 6.
Plasmacytoid dendritic cells (pDCs) detect viruses through toll-like receptor (TLR)7 and TLR9 and respond by secreting type I interferons (IFNs). Because TLR7 and TLR9 are present in endosomes, a mechanism is required to capture and deliver viruses to TLRs. A member of the sialic acid binding Ig-like lectin (Siglec) family, Siglec-H, has recently been identified as a specific surface marker for pDCs in mice. Siglec-H is endocytosed and can mediate the uptake of antigens for processing and presentation. Thus, Siglec-H might have a role in the capture of viruses or other pathogens for their delivery to intracellular TLRs. Paradoxically, Siglec-H also transmits intracellular signals through the associated adaptor DAP12, which reduces pDC responses to TLR ligands. In this review, we discuss models to explain the potential outcomes of Siglec-H engagement in the pDC secretion of type I IFN.
浆细胞样树突状细胞(pDCs)通过 Toll 样受体(TLR)7 和 TLR9 检测病毒,并通过分泌 I 型干扰素(IFN)做出反应。由于 TLR7 和 TLR9 存在于内体中,因此需要一种机制来捕获病毒并将其递送至 TLRs。唾液酸结合免疫球蛋白样凝集素(Siglec)家族的成员 Siglec-H 最近被确定为小鼠 pDCs 的特异性表面标志物。Siglec-H 可被内吞,并能介导抗原的摄取以进行加工和呈递。因此,Siglec-H 可能在捕获病毒或其他病原体并将其递送至细胞内 TLRs 方面发挥作用。矛盾的是,Siglec-H 还通过相关衔接蛋白 DAP12 传递细胞内信号,这会降低 pDCs 对 TLR 配体的反应。在本综述中,我们讨论了解释 Siglec-H 参与 pDCs 分泌 I 型干扰素潜在结果的模型。