Alternate header for print version


Licensing
Public Domain: This image is in the public domain and thus free of any copyright restrictions. However, as is the norm in scientific publishing and as a matter of courtesy, any user should credit the content provider for any public or private use of this image whenever possible. Learn more
tweet  
*CIL – Cell Image Library accession number. Please use this to reference an image.

CIL:35563*  Cite 
Description

Liver of a rat exposed to chemical carcinogens. Serial sections of the liver imaged by laser scanning confocal microscopy. F-actin (red) is in bile canaliculi at junctions of the hepatocytes, which are the large round cells arranged in a circular mass in the bottom center, in ductule cells, which are above and to the left of the hepatocytes, and in blood vessel endothelial cells, which are in the upper right and far left. Fibronectin (green) is in the tissue outside the hepatocytes. Bile ductule and/or oval cells are marked blue.

Technical Details

The liver of a rat fed a carcinogenic chemicals diet was cryo- and paraformaldehyde-fixed and frozen sections were prepared. The section was labeled with Cy 3 for OV-6, a marker for oval cells/bile ductile cells, Cy5 for fibronectin, and FITC for f-actin. Colors in this image were assigned to each probe by the Cell Imaging Library software. The confocal microscope was a BioRad MRC 600 with a Kr/Ar laser with lines at 488, 568, and 647 nm mounted on a Nikon Diaphot with 60X N.A. 1.4 phase 3 optics. Because the scan head only had two photomultiplier tubes, the filters had to be swapped out manually to collect a series of in register images of more than two fluorescent probes. The microscope was in the Analytical Imaging Facility of the Albert Einstein College of Medicine.

Biological Sources
NCBI Organism Classification
Rattus rattus
Cell Type
duct epithelial cell
hepatocyte
CL:1000036
Cellular Component
keratin filament
fibronectin
actin filament
Biological Context
Biological Process
cell proliferation
Molecular Function
toxin binding
Human Disease
liver carcinoma in situ
Attribution
Names
Phyllis Novikoff
Michael Cammer
Citation
Digital Object Identifier (DOI)
doi:10.7295/W9CIL35563
Archival Resource Key (ARK)
ark:/b7295/w9cil35563
Imaging
Image Type
recorded image
Image Mode
single point scanning
Parameters Imaged
fluorescence emission
Source of Contrast
distribution of a specific protein
Visualization Methods
Cy5
Cy3
Fluorescein (FITC)
Processing History
channels merged
Data Qualifiers
processed data
suitable for spatial measurements
Dimensions
Spatial Axis Image Size Pixel Size
X 768px 0.275µm
Y 512px 0.275µm
Z 13px 1µm