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Research Article Free access | 10.1172/JCI113296

Mitogenic effects of growth hormone in cultured human fibroblasts. Evidence for action via local insulin-like growth factor I production.

J J Cook, K M Haynes, and G A Werther

Department of Endocrinology and Diabetes, Royal Children's Hospital, Melbourne, Australia.

Find articles by Cook, J. in: JCI | PubMed | Google Scholar

Department of Endocrinology and Diabetes, Royal Children's Hospital, Melbourne, Australia.

Find articles by Haynes, K. in: JCI | PubMed | Google Scholar

Department of Endocrinology and Diabetes, Royal Children's Hospital, Melbourne, Australia.

Find articles by Werther, G. in: JCI | PubMed | Google Scholar

Published January 1, 1988 - More info

Published in Volume 81, Issue 1 on January 1, 1988
J Clin Invest. 1988;81(1):206–212. https://doi.org/10.1172/JCI113296.
© 1988 The American Society for Clinical Investigation
Published January 1, 1988 - Version history
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Abstract

We examined human growth hormone's (hGH) effect on mitogenesis in cultured human fibroblasts, and the role of local insulin-like growth factor I (IGF-I). With 0.5% human hypopituitary serum (HPS), hGH increased thymidine incorporation (TI) over serum-free medium dose responsively, with half-maximal effect at 10 ng/ml (0.5 nM) (hGH 127 +/- 8.8%; IGF-I 107 +/- 1.7% [SEM]) (n = 10). Similarly, with 0.5% HPS, hGH and IGF-I increased cell replication by 172 +/- 8.2% and 169 +/- 25%, respectively (n = 4). Specific IGF-I monoclonal antibody (Sm1.2) dose dependently blunted TI stimulated by 10 ng/ml hGH or IGF-I (at 1:1000, 38 +/- 6.5% and 30 +/- 14% reduction, respectively). Sm1.2 also reduced cell replication by both 10 ng/ml hGH and IGF-I, respectively, to 32% and 42% of stimulated values. Dexamethasone (0.1 microM) synergistically enhanced TI by both IGF-I and hGH. A 28-h time course for TI showed that hGH stimulated a similar peak to IGF-I, lagging in its effect by 4-10 h. We have provided further evidence that hGH stimulates growth of cultured human fibroblasts via local IGF-I production, consistent with IGF-I's paracrine-autocrine role.

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