Alternate header for print version


Licensing
This image is copyright protected. Any public or private use of this image is subject to prevailing copyright laws. Please contact the content provider of this image for permission requests.
tweet  
*CIL – Cell Image Library accession number. Please use this to reference an image.

CIL:7761*  Cite 
Description

A COS-1 cell (RIGHT) generating murine lukemia virus (MLV) labeled with Gag-YFP (red) and expressing dynamin2-CFP (green) in contact with XC target cell (LEFT) expressing mCAT1-CFP (green). MLV is transferred from infected dynamin-expressing Cos cells (green, to the right) to receptor expressing uninfected target cells (green, to the left). Four stages of retroviral transmission can be identified: First, the establishment of contact between the infected and uninfected cell. Second, contact-induced virus assembly at the sites of cell-cell contact. Third, transmission of virus via filopodial bridges. Fourth, downregulation of the cell-cell contact. Repeated rounds of establishment of contact, contact-induced virus assembly, and virus transmission are observed. Images were collected with a volocity spinning disc confocal microscope equipped with an environmental chamber (LIVE CELL; Pathology Devices) and a Nikon Perfect Focus using a 60X 1.4NA objective. A z-stack of red and green images was taken every 134 s and merged into a single file to generate the Video. The image resolution is 0.166619 um/pixel. Celldance 2008, 3rd Place Video: Sequential Waves of Retroviral Transmission from Cell to Cell

Biological Sources
NCBI Organism Classification
Chlorocebus sabaeus
Cell Line
COS-1
Kidney
Cellular Component
murine lukemia virus
Gag
dynamin2
Biological Context
Biological Process
transmission of virus
Attribution
Names
Jing Jin (Yale University School of Medicine)
Pubmed
19662089
Citation
Digital Object Identifier (DOI)
doi:10.7295/W9CIL7761
Archival Resource Key (ARK)
ark:/b7295/w9cil7761
Imaging
Image Type
recorded image
Image Mode
spinning disk confocal microscopy
Parameters Imaged
fluorescence emission
Source of Contrast
distribution of a specific protein
Visualization Methods
EYFP
ECFP
Processing History
color combine
Data Qualifiers
raw, unprocessed data
suitable for spatial measurements
Sample Preparation
Methods
living tissue
Relation To Intact Cell
dispersed cells in vitro
Dimensions
Spatial Axis Image Size Pixel Size
X 456px 0.167µm
Y 512px 0.167µm
Channel Wavelength
1 CFP, YFPµm
Time 134 seconds 240