File:Murid-Herpesvirus-4-Exploits-Dendritic-Cells-to-Infect-B-Cells-ppat.1002346.s003.ogv
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[edit]DescriptionMurid-Herpesvirus-4-Exploits-Dendritic-Cells-to-Infect-B-Cells-ppat.1002346.s003.ogv |
English: Bone marrow-derived DCs were infected with gM-eGFP+ MuHV-4 (3 p.f.u./cell) and imaged 6 h later by time-lapse confocal microscopy (Leica). Images were recorded every 8 sec over 7 min. The left-hand panel shows eGFP fluoresence and the right-hand panel the corresponding phase contrast image. At 6 h after exposure to MuHV-4, DCs show little late lytic gene expression. Thus the eGFP signal comes from the input virions. The non-adherent DCs correspond to those more activated prior to virus exposure, which are poorly infected and so remain eGFP-. The DCs taking up virions, and presumably becoming infected, show flattening, adherence to plastic and marked cytoplasmic motility. |
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Source | Video S1 from Gaspar M, May J, Sukla S, Frederico B, Gill M, Smith C, Belz G, Stevenson P (2011). "Murid Herpesvirus-4 Exploits Dendritic Cells to Infect B Cells". PLOS Pathogens. DOI:10.1371/journal.ppat.1002346. PMID 22102809. PMC: 3213091. | ||
Author | Gaspar M, May J, Sukla S, Frederico B, Gill M, Smith C, Belz G, Stevenson P | ||
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Date/Time | Thumbnail | Dimensions | User | Comment | |
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current | 01:24, 18 November 2012 | 7.1 s, 2,048 × 1,024 (6.7 MB) | Open Access Media Importer Bot (talk | contribs) | Automatically uploaded media file from Open Access source. Please report problems or suggestions here. |
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Author | Gaspar M, May J, Sukla S, Frederico B, Gill M, Smith C, Belz G, Stevenson P |
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Usage terms | http://creativecommons.org/licenses/by/3.0/ |
Image title | Bone marrow-derived DCs were infected with gM-eGFP+ MuHV-4 (3 p.f.u./cell) and imaged 6 h later by time-lapse confocal microscopy (Leica). Images were recorded every 8 sec over 7 min. The left-hand panel shows eGFP fluoresence and the right-hand panel the corresponding phase contrast image. At 6 h after exposure to MuHV-4, DCs show little late lytic gene expression. Thus the eGFP signal comes from the input virions. The non-adherent DCs correspond to those more activated prior to virus exposure, which are poorly infected and so remain eGFP-. The DCs taking up virions, and presumably becoming infected, show flattening, adherence to plastic and marked cytoplasmic motility. |
Software used | Xiph.Org libtheora 1.1 20090822 (Thusnelda) |
Date and time of digitizing | 2011-11 |