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Journal of Lipid Research, Vol 36, 868-875, Copyright © 1995 by Lipid Research, Inc.
SA Hazen, WA Rowe and CJ Lynch
Cell biological techniques requiring cells attached to surfaces, such as
monolayer cell culture, microspectrofluorometry, and confocal microscopy,
have not been readily available for use on adipocytes because they float
and tend to lyse when attached to charged non- biological surfaces. A new
method for attaching freshly isolated rodent adipocytes to thermanox
plastic surfaces using Matrigel (a defined mixture of extracellular matrix
components that resembles the basal lamina surrounding adipocytes in vivo)
is described. The method takes advantage of an unusual physical
characteristic of Matrigel, i.e., that it is a liquid at cold temperatures
and a hydrated gel at higher temperatures. To attach the isolated cells,
chilled thermanox plastic coverslips were coated with a thin uniform layer
of ice-cold Matrigel and inverted into warm floating adipocytes. Adipocytes
floated up against the liquid Matrigel and became immediately attached when
the Matrigel changed to a gel in response to the warmth of the cells and
media. Cell volume measurements of the attached versus freshly isolated
cells indicate no significant difference in the centroid cell volume of the
attached cells. This indicates that the method does not select for small or
large cells. Adipocytes maintained for 6 days in culture did not display
any change in their size or differentiated microscopic appearance. The
relative concentrations of major proteins in silver- stained SDS-PAGE gels
and several differentiation state-dependent proteins, including ATP-citrate
lyase, carbonic anhydrase III (CA III), adipocyte lipid binding protein
(ALBP), and pyruvate carboxylase, were examined. No significant change was
observed in the relative concentrations of these proteins when the
matrigel-cultured adipocytes were compared to freshly isolated
cells.(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
Monolayer cell culture of freshly isolated adipocytes using extracellular basement membrane components
Department of Cellular and Molecular Physiology, Milton S. Hershey Medical Center and College of Medicine, Pennsylvania State University, Hershey 17033, USA.
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