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吞噬携带分枝杆菌抗原的凋亡巨噬细胞的树突状细胞通过交叉呈递激活CD8 T细胞。

Dendritic cells that phagocytose apoptotic macrophages loaded with mycobacterial antigens activate CD8 T cells via cross-presentation.

作者信息

Espinosa-Cueto Patricia, Magallanes-Puebla Alejandro, Castellanos Carlos, Mancilla Raul

机构信息

Departamento de Inmunología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Mexico City, Mexico.

出版信息

PLoS One. 2017 Aug 2;12(8):e0182126. doi: 10.1371/journal.pone.0182126. eCollection 2017.

DOI:10.1371/journal.pone.0182126
PMID:28767693
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5540487/
Abstract

While homeostatic apoptosis is immunologically silent, macrophage apoptosis during Mycobacterium tuberculosis infection can potentially induce an immune response against the mycobacteria. To examine the role of dendritic cells in this response, macrophage apoptosis was induced by incubating the macrophage with cell wall extracts of mycobacteria expressing LpqH. The apoptogenic proteins of the cell wall extracts were engulfed by the macrophage and then were translocated from the cytosol to the nuclei of the dying cells. Dendritic cells that engulfed the apoptotic macrophages acquired an immunogenic phenotype that included upregulation of MHC-I, increased expression of the costimulatory molecules, CD40, CD80, and CD86, and increased production of IL-12, IL-10, TNF-α, and TGF-β. In addition, the dendritic cells triggered a proliferative response of CD8+ T cells with IFN-γ production via cross-presentation. Taken together, these findings support a model in which phagocytosis of whole apoptotic cells carrying mycobacterial antigens promotes a potentially protective immune response.

摘要

虽然稳态凋亡在免疫上是沉默的,但结核分枝杆菌感染期间巨噬细胞凋亡可能会诱导针对分枝杆菌的免疫反应。为了研究树突状细胞在这种反应中的作用,通过将巨噬细胞与表达LpqH的分枝杆菌细胞壁提取物孵育来诱导巨噬细胞凋亡。细胞壁提取物的凋亡蛋白被巨噬细胞吞噬,然后从细胞质转移到垂死细胞的细胞核中。吞噬凋亡巨噬细胞的树突状细胞获得了免疫原性表型,包括MHC-I上调、共刺激分子CD40、CD80和CD86表达增加,以及IL-12、IL-10、TNF-α和TGF-β产生增加。此外,树突状细胞通过交叉呈递引发CD8+T细胞的增殖反应并产生IFN-γ。综上所述,这些发现支持了一个模型,即携带分枝杆菌抗原的完整凋亡细胞的吞噬作用促进了潜在的保护性免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cf8/5540487/6c79b92b3039/pone.0182126.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cf8/5540487/792d040c69e9/pone.0182126.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cf8/5540487/94c9bb026b27/pone.0182126.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cf8/5540487/3a3d25a34bef/pone.0182126.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cf8/5540487/36066837cb05/pone.0182126.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cf8/5540487/9ea20eb769b6/pone.0182126.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cf8/5540487/6c79b92b3039/pone.0182126.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cf8/5540487/792d040c69e9/pone.0182126.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cf8/5540487/94c9bb026b27/pone.0182126.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cf8/5540487/3a3d25a34bef/pone.0182126.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cf8/5540487/36066837cb05/pone.0182126.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cf8/5540487/9ea20eb769b6/pone.0182126.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cf8/5540487/6c79b92b3039/pone.0182126.g006.jpg

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