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

CIL:25537*  Cite 

The final morphogenesis of the cardiac outflow tract (OFT) depends on coordinated cell-cell interactions among the heart tip, migrating heart-anchoring cells (HANCs) and the dorsally growing cardiac outflow muscles (COMs). This is a three-dimensional reconstruction of the cardiac outflow tract (horizontal rotation) from stage-16 wild-type embryos stained for Ladybird early (Lbe; blue), Msp300 (green), and Myocyte enhancer factor 2 (Mef2; red). HANC cells (in blue) overlap dorsally the most anterior aorta. The COM muscles (in green) are attached on both sides to the most anterior Lbe-expressing cardioblasts (at this stage Lbe expression in the cardioblasts and pericardial cells is very week, and rendering Lbe signal visible resulted in an increased background). Note that ventrally to the tip of aorta are located cephalic vascular rudiment cells (cvr), which are Tin-positive, Dmef2-negative. Movie is SI Movie 1B in Proc Natl Acad Sci USA (2008) 105: 2475-2480. Movies from this publication include CIL# 25536, 25537, 25538, 25539, 25540, 25541.

Technical Details

Stage 16 embryos were stained with primary antibodies: mouse anti-Lbe, rabbit anti-Mef2, guinea pig anti-Msp300. Species-specific secondary antibodies were conjugated to Alexa Fluor 488, Cy3 or Cy5. The triple stained embryos were visualized using a Zeiss LSM 510 Meta confocal microscope. Images representing 0.5 mm optical sections were compiled and processed by Volocity software (Improvision).

Biological Sources
NCBI Organism Classification
Drosophila melanogaster
Cell Type
cardioblast (sensu Arthropoda)
pericardial cell
cardiac outflow muscle
heart-anchoring cells
cephalic vascular rudiment cells
Cellular Component
actin cytoskeleton
integrin complex
Monika Zmojdzian
Jean Philippe Da Ponte
Krzysztof Jagla
Proc Natl Acad Sci USA (2008) 105: 2475-2480.
Digital Object Identifier (DOI)
Archival Resource Key (ARK)
Grouping This image is part of a group.
Image Type
recorded image
3D reconstruction
Image Mode
single-spot confocal microscopy
Parameters Imaged
fluorescence emission
Source of Contrast
distribution of a specific protein
Visualization Methods
primary antibody plus labeled secondary antibody
Alexa Fluor 488
Processing History
3D reconstruction
Data Qualifiers
processed data
Sample Preparation
formaldehyde fixed tissue
detergent permeabilized
Relation To Intact Cell
whole mounted tissue
Spatial Axis Image Size Pixel Size
X 784px ——
Y 576px ——
Z —— 500µm