Horm Metab Res 2000; 32(11/12): 555-559
DOI: 10.1055/s-2007-978685
Original

© Georg Thieme Verlag Stuttgart · New York

IGF-I- and IGFBP-3-Expression in Cultured Human Preadipocytes and Adipocytes

M. Wabitsch1 , E. Heinze1 , K.-M. Debatin1 , W. F. Blum2 , 3
  • 1Department of Pediatrics, University of Ulm, Ulm, Germany
  • 2Department of Pediatrics, University of Leipzig, Leipzig, Germany
  • 3Lilly Deutschland, Bad Homburg, Germany
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Publikationsverlauf

2000

2000

Publikationsdatum:
19. April 2007 (online)

The expression and secretion of IGF-I and IGFBP-3 were investigated in cultured human preadipocytes and in in vitro differentiated adipocytes derived from human subcutaneous adipose tissue under chemically defined culture conditions. Human preadipocytes expressed mRNAs for IGF-I and IGFBP-3 and secreted the corresponding proteins into the culture medium as measured by sensitive radioimmunoassays. In human adipocytes; specific mRNA-expression was comparable to that found in preadipocytes, but IGF-I secretion was increased 10-fold (3.87 ± 0.69 vs. 0.41 ± 0.11 ng/ml/106 cells/48hrs, p < 0.05) and IGFBP-3 secretion 2.5-fold (7.34 ± 1.15 vs. 3.27 ± 0.38 ng/ml/106 cells/48 hrs, p < 0.05) in the presence of adipogenic medium probably resulting in an increase of unbound IGF-I. Under serum-free, chemically defined conditions human growth hormone (hGH) and insulin were found to be positive regulators and cortisol was found to be a negative regulator of IGF-I and IGFBP-3 secretion in preadipocytes. In cultured human adipocytes, hGH showed no effect on IGF-I and IGFBP-3 secretion, whereas insulin stimulated and cortisol inhibited the secretion of both proteins. We conclude that IGF-I and IGFBP-3 may not only exert their actions in human adipose tissue via circulation, but also in an auto/paracrine way.