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Journal of Lipid Research, Vol 26, 1187-1195, Copyright © 1985 by Lipid Research, Inc.
P Pettersson, RL Van, P Lonnroth, P Bjorntorp and U Smith
Binding, degradation, and antilipolytic effect of insulin were studied
during the differentiation of preadipocytes into unilocular adipocytes. The
precursor cells were isolated from the stromal-vascular fraction of adult
rat epididymal fat pads and were cultured according to methods previously
described. Under appropriate conditions the cells attained full
morphological maturation after 6 days. A gradual increase in insulin
binding was found concomitant with the morphological development of the
preadipocytes into adipocytes. This increase was due to an enhanced number
of binding sites whether expressed per cell or per unit cell surface area.
The presence of a high insulin concentration (1.67 micrograms/ml or 278 nM)
in the culture medium did not prevent this effect. The receptor density,
expressed per unit surface area, was higher in the newly developed
univacuolar cells than in mature fat cells from the same rat. The increased
receptor density was also reflected by a leftward shift in the
dose-response curve for the antilipolytic effect of insulin. In parallel
with the increased binding, insulin degradation also increased. The
lipolytic response to catecholamine also showed a gradual increase with
development. When expressed per unit surface area, newly formed cells
exhibited a considerably greater response (approximately 3.4 times) than
mature cells from the same animals. The maximal antilipolytic effect of
insulin in new cells was of the same order as in old cells when the data
were expressed per unit cell surface area. Thus, the data show that
developing adipocyte precursors gain membrane properties similar to those
of mature fat cells. This cell system may serve as a useful model for
studying receptor formation and factors that regulate hormone
responsiveness.
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Insulin binding in differentiating rat preadipocytes in culture
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