Horm Metab Res 1984; 16(8): 439-444
DOI: 10.1055/s-2007-1014811
Originals

© Georg Thieme Verlag, Stuttgart · New York

Pygmy Mouse Fibroblasts in Tissue Culture: Evaluation of Multiplication Stimulating Activity (MSA) Receptors and Growth Responses to MSA

G. P. August1 , S. P. Nissley2 , R. M. White3
  • 1Department of Endocrinology and Metabolism, Children's Hospital National Medical Center, Washington, D.C., U.S.A.
  • 2Metabolism Branch, National Cancer Institute, Washington, D.C., U.S.A.
  • 3Vincent Lombardi Cancer Center, Georgetown University Medical Center, Washington, D.C., U.S.A.
Further Information

Publication History

1982

1983

Publication Date:
14 March 2008 (online)

Summary

The pygmy mouse has been proposed as a model for growth hormone resistance; it has normal serum somatomedin levels and does not respond to growth hormone treatment. In order to determine if the growth impairment is caused by a defect in somatomedin binding or in postreceptor action of somatomedin we compared fibroblasts derived from pygmy mice with those from normal appearing littermates. Using multiplication-stimulating activity (MSA) as a model somatomedin we found a normal Ka of binding to the cell surface MSA receptor but a significantly increased number of MSA receptors on the fibroblasts derived from pygmy mice. Studies of thymidine incorporation into DNA failed to demonstrate a difference between pygmy and normal fibroblasts in their responses to MSA alone, but there was a significantly greater thymidine incorporation into the DNA of normal fibroblasts when both competence factor (plateletderived growth factor) and progression factors (somatomedins and growth hormone deficient platelet-poor plasma) were present in the test medium. On the other hand, cell proliferation studies did not demonstrate a consistent difference in the growth rate of normal versus pygmy fibroblasts. The data support the conclusion that the impaired growth of the pygmy mouse in vivo may be caused by factors which lie outside of the growth hormone-somato-medin pathway.

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