Antigen Processing and Presentation by Dendritic Cells: Cell Biological Mechanisms

Author(s):  
Ira Mellman
1999 ◽  
Vol 96 (26) ◽  
pp. 15056-15061 ◽  
Author(s):  
L. Santambrogio ◽  
A. K. Sato ◽  
G. J. Carven ◽  
S. L. Belyanskaya ◽  
J. L. Strominger ◽  
...  

PLoS ONE ◽  
2007 ◽  
Vol 2 (9) ◽  
pp. e957 ◽  
Author(s):  
Marielle C. Gold ◽  
Tammie L. Robinson ◽  
Matthew S. Cook ◽  
Laura K. Byrd ◽  
Heather D. Ehlinger ◽  
...  

2010 ◽  
Vol 84 (17) ◽  
pp. 8964-8969 ◽  
Author(s):  
Mélanie Lambotin ◽  
Thomas F. Baumert ◽  
Heidi Barth

ABSTRACT Dendritic cells (DCs) are of pivotal importance for the initiation of immune responses to control and eliminate viral infections. The molecular mechanisms of hepatitis C virus (HCV) antigen uptake and processing by blood DCs are poorly defined. Here we show that human blood DC subsets acquire HCV independent of the classical HCV entry factors. Following HCV uptake, human plasmacytoid and myeloid DC subsets deliver HCV antigen into distinct endocytotic compartments, which are dedicated to presentation to CD4+ or CD8+ T cells. Our findings support a model of HCV antigen processing and presentation in which DC subsets fulfill distinct functions.


2020 ◽  
Vol 21 (3) ◽  
pp. 687
Author(s):  
Marlene Bravo-Parra ◽  
Marina Arenas-Padilla ◽  
Valeria Bárcenas-Preciado ◽  
Jesús Hernández ◽  
Verónica Mata-Haro

MicroRNAs (miRNAs) mediate the regulation of gene expression. Several reports indicate that probiotics induce miRNA-mediated immunomodulation at different levels, such as cytokine production and the up-regulation of several markers related to antigen presentation in antigen-presenting cells. The objective of this work was to identify target genes of miRNAs that are involved in the processing and presentation of antigens in monocyte-derived dendritic cells (moDCs) stimulated with the probiotic Bifidobacterium animalis ssp. lactis BB12 (BB12). First, an in silico prediction analysis for a putative miRNA binding site within a given mRNA target was performed using RNAHybrid software with mature sequences of differentially expressed miRNAs retrieved from a Genbank data set that included BB12-stimulated and unstimulated porcine monocytes. From them, 23 genes resulted in targets of 19 miRNAs, highlighting miR-30b-3p, miR-671-5p, and miR-9858-5p, whose targets were costimulatory molecules, and were overexpressed (p < 0.05) in BB12-stimulated moDCs. The analysis of moDCs showed that the percentage of cells expressing SLA-DR+CD80+ decreased significantly (p = 0.0081) in BB12-stimulated moDCs; interleukin (IL)-10 production was unchanged at 6 h but increased after 24 h of culture in the presence of BB12 (p < 0.001). In summary, our results suggest that SLA-DR and CD80 can be down-regulated by miRNAs miR-30b-3p, miR-671-5p, and miR-9858-5p, while miR-671-5p targets IL-10.


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