Fleeton Marina N, Contractor Nikhat, Leon Francisco, Wetzel J Denise, Dermody Terence S, Kelsall Brian L
Laboratory of Molecular Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Building 10, Room 11N228, Bethesda, MD 20892, USA.
J Exp Med. 2004 Jul 19;200(2):235-45. doi: 10.1084/jem.20041132.
We explored the role of Peyer's patch (PP) dendritic cell (DC) populations in the induction of immune responses to reovirus strain type 1 Lang (T1L). Immunofluorescence staining revealed the presence of T1L structural (sigma1) and nonstructural (sigmaNS) proteins in PPs of T1L-infected mice. Cells in the follicle-associated epithelium contained both sigma1 and sigmaNS, indicating productive viral replication. In contrast, sigma1, but not sigmaNS, was detected in the subepithelial dome (SED) in association with CD11c(+)/CD8alpha(-)/CD11b(lo) DCs, suggesting antigen uptake by these DCs in the absence of infection. Consistent with this possibility, PP DCs purified from infected mice contained sigma1, but not sigmaNS, and PP DCs from uninfected mice could not be productively infected in vitro. Furthermore, sigma1 protein in the SED was associated with fragmented DNA by terminal deoxy-UTP nick-end labeling staining, activated caspase-3, and the epithelial cell protein cytokeratin, suggesting that DCs capture T1L antigen from infected apoptotic epithelial cells. Finally, PP DCs from infected mice activated T1L-primed CD4(+) T cells in vitro. These studies show that CD8alpha(-)/CD11b(lo) DCs in the PP SED process T1L antigen from infected apoptotic epithelial cells for presentation to CD4(+) T cells, and therefore demonstrate the cross-presentation of virally infected cells by DCs in vivo during a natural viral infection.
我们探究了派尔集合淋巴结(PP)树突状细胞(DC)群体在对呼肠孤病毒1型朗株(T1L)免疫应答诱导中的作用。免疫荧光染色显示,在T1L感染小鼠的PP中存在T1L结构蛋白(sigma1)和非结构蛋白(sigmaNS)。滤泡相关上皮中的细胞同时含有sigma1和sigmaNS,表明病毒进行了有效的复制。相比之下,仅在与CD11c(+)/CD8alpha(-)/CD11b(lo) DC相关的上皮下圆顶(SED)中检测到sigma1,而未检测到sigmaNS,这表明这些DC在未感染的情况下摄取了抗原。与这种可能性一致的是,从感染小鼠中纯化的PP DC含有sigma1,但不含有sigmaNS,并且未感染小鼠的PP DC在体外不能被有效感染。此外,通过末端脱氧尿苷三磷酸缺口末端标记染色、活化的半胱天冬酶-3和上皮细胞蛋白细胞角蛋白检测发现,SED中的sigma1蛋白与片段化DNA相关,这表明DC从感染的凋亡上皮细胞中捕获T1L抗原。最后,来自感染小鼠的PP DC在体外激活了经T1L致敏的CD4(+) T细胞。这些研究表明,PP SED中的CD8alpha(-)/CD11b(lo) DC处理来自感染的凋亡上皮细胞的T1L抗原,以呈递给CD4(+) T细胞,因此证明了在自然病毒感染期间DC在体内对病毒感染细胞的交叉呈递。