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Control of growth by the somatropic axis: Growth hormone and the insulin-like growth factors have related and independent roles

Journal

ANNUAL REVIEW OF PHYSIOLOGY
Volume 63, Issue -, Pages 141-164

Publisher

ANNUAL REVIEWS
DOI: 10.1146/annurev.physiol.63.1.141

Keywords

conditional knockouts; somatomedin hypothesis; cell proliferation

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The traditionally accepted theory has been that most of the biological effects of growth hormone (GH) are mediated by circulating (endocrine) insulin-like growth factor-I (IGF-I). This dogma was modified when it was discovered that most tissues express IGF-I that can act via an autocrine/paracrine fashion. In addition, both GH and IGF-I had independent effects on various target tissues. Using tissue-specific gene deletion of IGF-I in the liver, it has been shown that circulating IGF-I is predominantly liver-derived but is not essential for normal postnatal growth. Therefore, it is proposed that non-hepatic tissue-derived IGF-I may be sufficient for growth and development. Thus the original somatomedin hypothesis has undergone further modifications.

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