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CIL:37912*  Cite 

Apoptotic cells produce and transmit the bioactive lipid sphingosine-1-phosphate (S1P) during extrusion. In this confocal Z-series, an antagonist to the S1P receptor, S1P2, was used to plock signaling. High levels of S1P accumulate in the dying, unextruded cells but not in surrounding cells. The nucleus is in blue, the actin-myosin ring at the basolateral surface is in red and S1P is in green.

Technical Details

Cultured HBE monolayers were treated with 10 µM JTE-013 for 10 min. To induce apoptosis, monolayers were exposed to 1,200 µJ/cm2 UV254 irradiation in a UV series II (Spectroline) and incubated for 2 h before fixation. Cells were fixed with 4% formaldehyde in PBS, permeabilized with 0.5% Triton, blocked and incubated with primary antibody for 1 h (50 µg/ml anti-S1P mAb (LPath Inc.)). Secondary antibody was Alexa Fluor 488 goat anti–mouse IgG. Actin was detected with Alexa Fluor 568–phalloidin (Invitrogen). DNA was detected with 5 µM DRAQ5 (Axxora). Confocal micrographs were obtained using a microscope (TCS SP5; Leica) with a 63x oil lens with an electron-multiplied cooled CCD camera 1,000 x 1,000, 8 x 8 mm2 driven by the IQ software (Andor Technologies). ImageJ was used to stack confocal sections into Z series that were then color combined and reconstructed into 3D image using MetaMorph (GE Healthcare). All images were processed further using ImageJ, Photoshop (Adobe), Illustrator (Adobe), and Quicktime Pro (Quicktime) software. This Z-series corresponds to Fig 4E from J Cell Biol. 2011. 193(4): 667-676

Biological Sources
NCBI Organism Classification
Homo sapiens
Cell Type
epithelial cell
Cell Line
Cellular Component
cortical actin cytoskeleton
Biological Context
Biological Process
apoptotic process
actomyosin structure organization
Molecular Function
protein binding
Yapeng Gu
Tetyana Forostyan
Roger Sabbadini
Jody Rosenblatt
J Cell Biol. 2011. 193(4): 667-676
Digital Object Identifier (DOI)
Archival Resource Key (ARK)
Grouping This image is part of a group.
Image Type
recorded image
Image Mode
single-spot confocal microscopy
fluorescence microscopy
Parameters Imaged
fluorescence emission
Source of Contrast
distribution of a specific protein
distribution of epitope
compartmentalization of stain or label
Visualization Methods
Alexa Fluor 488
Alexa Fluor 568
Processing History
unprocessed raw data
Data Qualifiers
raw, unprocessed data
suitable for spatial measurements
Sample Preparation
formaldehyde fixed tissue
detergent permeabilized
Relation To Intact Cell
dispersed cells in vitro
Spatial Axis Image Size Pixel Size
X 1024px 1µm
Y 1024px 1µm
Z 43px ——