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Journal of Lipid Research, Vol 22, 1053-1059, Copyright © 1981 by Lipid Research, Inc.
TD Etherton and CS Chung
The technique of Rodbell (J. Biol. Chem. 239: 375) was modified
considerably in order to isolate swine adipocytes without rupturing large
cells. Cell size and diameter distributions were the same for adipocytes
fixed with OsO4 following isolation with collagenase and adipoctes
liberated from OsO4-fixed adipose tissue slices. Lipogenic rates were
greater for isolated adipocytes compared with thin adipose tissue slices at
low (0.5 mM) and high (10 mM) glucose concentrations (cells = 307 and 1100;
slices = 139 and 744 nMoles glucose leads to lipid/10(6) cells/hr for 0.5
and 10 mM glucose, respectively, P less than 0.001). Similar differences
were found for glucose oxidation. Sensitivity to insulin was determined by
measuring the stimulation of lipogenesis and glucose oxidation in the
presence of 0, 1, 5, 25, and 100 ng/ml of purified porcine insulin at low
(0.5 mM) and high (10 mM) glucose concentrations. Relative to basal
incubations, the addition of insulin caused similar increases in glucose
oxidation and lipogenesis for isolated adipocytes and adipose tissue slices
when glucose concentration was 10 mM. These results indicate 1) that
isolated swine adipocytes can be prepared without alterations in cell size
or diameter distribution, and 2) that isolated adipocytes have higher rates
of glucose oxidation and lipogenesis from glucose even though they retain a
similar in vitro sensitivity to insulin.
ARTICLES
Preparation, characterization, and insulin sensitivity of isolated swine adipocytes: comparison with adipose tissue slices
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