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*CIL – Cell Image Library accession number. Please use this to reference an image.

CIL:9530*  Cite 
Description

Adhesion dynamics in a migrating CHO K1 cell. CHO K1 cells expressing paxillin-mEGFP were plated onto coverslips that were preincubated with a solution of 5 ug/ml fibronectin overnight at 4o C. The cells were visualized at 60x (1.45NA) with an Olympus IX70 inverted microscope using Total Internal Reflection Optics (through the objective mode) equipped with a Qimaging Retiga Exi CCD camera (0.1073 microns/pixel). Images were acquired every 5 seconds for a total of 15 minutes. Note the formation of small, nascent adhesions near the leading edge of protrusions. These adhesions form (in the lamellipodium) and their formation is coupled to actin polymerization. Many adhesions turnover (at the lamellipodium/lamellum interface), as the protrusion proceeds. Some adhesions also elongate and grow (mature), particularly during pauses in protrusion. The fraction of adhesions that elongate, and the rate at which they do so, is cell type dependent. Note also, the sliding and disassembly of adhesions in retracting regions of the cell. The movie was taken by Colin Choi in the Rick Horwitz laboratory (University of Virginia).

Biological Sources
NCBI Organism Classification
Cricetulus griseus
Cell Type
epithelial cell
Cell Line
CHO-K1
Cellular Component
cell-substrate adherens junction
focal adhesion
Attribution
Names
Colin K. Choi
Alan Rick Horwitz
Pubmed
19160484
Pubmed
20729930
Citation
Digital Object Identifier (DOI)
doi:10.7295/W9CIL9530
Archival Resource Key (ARK)
ark:/b7295/w9cil9530
Imaging
Image Type
recorded image
Image Mode
TIRF
Parameters Imaged
fluorescence emission
Source of Contrast
distribution of a specific protein
Visualization Methods
EGFP
Processing History
unprocessed raw data
Sample Preparation
Methods
dispersed cells in vitro
Relation To Intact Cell
unfixed tissue
Dimensions
Spatial Axis Image Size Pixel Size
X 600px 0.1073µm
Y 600px 0.1073µm
Time 5 seconds 15 min