Differentiation under the control of insulin of rat preadipocytes in primary culture. Isolation of homogeneous cellular fractions by gradient centrifugation

Biochim Biophys Acta. 1983 Jun 2;762(3):437-44. doi: 10.1016/0167-4889(83)90009-5.


Using a density gradient medium (Percoll) we succeeded in isolating homogeneous cell populations from the stromal-vascular fraction of the inguinal tissue of 3-day-old rats. In primary culture, in medium 199 supplemented with 10% fetal calf serum and 5.5 mM glucose, almost complete differentiation (90%) of these fractions was obtained for the first time in presence of a physiological concentration of insulin (10(-9) M). During the adipose conversion, insulin markedly enhanced the activities of glycerol-3-phosphate dehydrogenase and acid: CoA ligase. When VLDL and heparin were added with insulin to the medium, this effect was not potentiated. On the contrary, VLDL and heparin in presence of insulin increased the triglyceride content of the cells. With VLDL and heparin only, the biochemical and morphological characteristics of the cells were very similar to those observed in control culture. The heavier fraction was morphologically heterogeneous and did not undergo the adipose conversion to the same extent as the two lighter fractions. It was concluded that this model could be helpful in studying the proliferation and the differentiation of preadipocytes at an early stage of development.

MeSH terms

  • Adipose Tissue / cytology
  • Adipose Tissue / metabolism*
  • Animals
  • Cell Differentiation / drug effects
  • Cell Fractionation
  • Cells, Cultured
  • Centrifugation, Density Gradient
  • Coenzyme A Ligases / metabolism
  • Diglycerides / metabolism
  • Glycerolphosphate Dehydrogenase / metabolism
  • Heparin / pharmacology
  • Insulin / isolation & purification*
  • Insulin / physiology
  • Lipoproteins, VLDL / pharmacology
  • Rats
  • Repressor Proteins*
  • Saccharomyces cerevisiae Proteins*
  • Triglycerides / metabolism


  • Diglycerides
  • Insulin
  • Lipoproteins, VLDL
  • Repressor Proteins
  • Saccharomyces cerevisiae Proteins
  • Triglycerides
  • Heparin
  • Glycerolphosphate Dehydrogenase
  • Coenzyme A Ligases
  • FAA2 protein, S cerevisiae
  • long-chain-fatty-acid-CoA ligase