LeibundGut-Landmann Salomé, Waldburger Jean-Marc, Reis e Sousa Caetano, Acha-Orbea Hans, Reith Walter
Department of Pathology and Immunology, University of Geneva Medical School, 1211 Geneva, Switzerland.
Nat Immunol. 2004 Sep;5(9):899-908. doi: 10.1038/ni1109. Epub 2004 Aug 22.
Major histocompatibility complex (MHC) class II-restricted antigen presentation is essential for the function of dendritic cells (DCs). We show here that plasmacytoid DCs (pDCs) differ from all other DC subsets with respect to expression of CIITA, the 'master regulator' of MHC class II genes. The gene encoding CIITA is controlled by three cell type-specific promoters: pI, pIII and pIV. With gene targeting in mice, we demonstrate that pDCs rely strictly on the B cell promoter pIII, whereas macrophages and all other DCs depend on pI. The molecular mechanisms driving MHC class II expression in pDCs are thus akin to those operating in lymphoid rather than myeloid cells.
主要组织相容性复合体(MHC)II类限制性抗原呈递对于树突状细胞(DC)的功能至关重要。我们在此表明,浆细胞样DC(pDC)在MHC II类基因的“主调节因子”CIITA的表达方面与所有其他DC亚群不同。编码CIITA的基因由三种细胞类型特异性启动子控制:pI、pIII和pIV。通过小鼠基因靶向,我们证明pDC严格依赖B细胞启动子pIII,而巨噬细胞和所有其他DC则依赖pI。因此,驱动pDC中MHC II类表达的分子机制类似于在淋巴细胞而非髓细胞中起作用的机制。