DIFFERENTIAL REGULATION OF INSULIN-LIKE GROWTH-FACTOR-I (IGF-I) AND IGF BINDING PROTEIN-1 MESSENGER RIBONUCLEIC-ACIDS BY AMINO-ACID AVAILABILITY AND GROWTH-HORMONE IN RAT HEPATOCYTE PRIMARY CULTURE

To determine the mechanisms involved in the nutritional regulation of insulin-like growth factor I (IGF-I) production and action, we studied the regulation of IGF-I and IGF-Binding Protein 1 (IGFBP-1) gene expr ession by GH and amino acid availability in rat hepatocyte primary cul ture. Hepatocytes were isolated by in situ collagenase perfusion and c ultured on Matrigel in serum-free medium containing insulin and hydroc ortisone. Rat GH (500 ng/ml) increased IGF-I messenger RNA (mRNA) abun dance 6.9-fold at 24 h, as measured by Northern Blot using an IGF-I-sp ecific riboprobe. In contrast, IGFBP-1 mRNA levels were decreased by 4 1% after 24 h of rat GH treatment. Hepatocytes were incubated for 24 h in three media differing in their amino acid concentrations::0.2x, 1x , and 5x the normal rat plasma concentration. Amino acid deprivation ( 0.2x) decreased the abundance of IGF-I mRNAs (-56% after 24 h), wherea s amino acid excess (5x) increased it (+70%) in comparison to the Ix m edium. In contrast, amino acid deprivation increased IGFBP-1 mRNA abun dance (+69%), whereas excess decreased it (-75%). Studies of the inter action between GH and amino acids, accomplished by the simultaneous ma nipulation of the two, suggest that each factor modulates the IGF-I mR NA and the IGFBP-1 mRNA and protein response to the other. We conclude that the IGF-I and IGFBP-1 genes are regulated in opposite ways by GH and amino acid availability. Our observations suggest that amino acid s and GH regulate the production of IGF-I directly and exert indirect effects on IGF-I action by regulating the production of IGFBP-1.