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Description

Intracellular dye injections of protoplasmic astrocytes from the CA1 region of hippocampus of 3 week old rat reveals highly ramified spongiform processes that span territories with minimal overlap. Astrocytes were filled with Lucifer Yellow (green) and Alexa 568 (red) Optical sections were generated with a single photon confocal microscope.

Technical Details

Male Sprague Dawley rats, 3 weeks of age, were anaesthetized and perfused transcardially with with Ringer's solution (37°C), followed by 4% paraformaldehyde (PFA) in PBS (37°C, pH 7.4). Tissue was sectioned (100 µm thick) using a vibratome, and injected with a BX50WI microscope (Olympus, Melville, NY) and, using infrared differential interference contrast videomicroscopy,cells with a small diameter soma (approx. 7–11µm) in the stratum radiatum of CA1 were located and impaled with glass micropipettes filled with either 5% aq. LY, 20mM AlexaFluor 568 in 200mM KCl, or 20mM AlexaFluor 488 in 200mM KCl. The astrocytes were filled using a 0.5 Hz pulses of current until all of the processes were brightly fluorescent. After several astrocytes were filled, a slice was placed in the 4% PFA overnight at 4°C. Slices were then imaged after coverslipping in Gelvatol. Confocal images were acquired with a BioRad Radiance2000 (Hercules, CA) attached to a Nikon E600FN (Kanagawa, Japan) microscope equipped with a Nikon (Tokyo, Japan) 60× oil objective (NA 1.4). Optical resolution of the z-axis, 0.25µm. Additional details are provided in Bushong EA, Martone ME, Ellisman MH. Maturation of astrocyte morphology and the establishment of astrocyte domains during postnatal hippocampal development. Int J Dev Neurosci. 2004 Apr;22(2):73-86.

Biological Sources

NCBI Organism Classification
Rattus
(Old World rats)
Cell Type
astrocyte
Cellular Component
cell projection cytoplasm
cell body

Biological Context

Biological Process
forebrain astrocyte development

Attribution

Names
Eric A. Bushong
Maryann E. Martone
Mark H. Ellisman
Link
CCDB ID 1009
Pubmed
15036382

Grouping

This image is representative of a group of similar images.

Imaging

Image Type
recorded image
Imaging Mode
confocal microscopy
Parameters Imaged
fluorescence emission
Source of Contrast
intracellular filling
Visualization Methods
lucifer yellow
Alexa Fluor 568
Data Qualifiers
processed data
suitable for spatial measurements

Sample Preparation

Methods
formaldehyde fixed tissue
Relation To Intact Cell
vibratome-sectioned tissue

Dimensions

Spatial Axis Image Size Pixel Size
X 1052px 0.053623μm
Y 1052px 0.053623μm
*CIL – Cell Image Library accession number. Please use this to reference an image.