{"title":"Insulin-like growth factor I (IGF I) induces cortisol production in bovine adrenocortical cells in primary culture","authors":"Marie T. Pham-Huu-Trung, Michel Binoux","doi":"10.1016/0022-4731(90)90176-S","DOIUrl":null,"url":null,"abstract":"<div><p>The effects of a physiological dose of IGF I (40 ng/ml ≈ 5 × 10<sup>−9</sup> M) on steroidogenesis were studied in bovine adrenal fasciculata cells cultured in serum-free McCoy's medium. They were compared with those of a single dose of ACTH (0.25 ng/ml ≈ 10<sup>−10</sup> M) at approximately the concentration inducing half-maximal stimulation. With IGF I, steroidogenesis commenced after 48 h culture and progressively increased throughout the 96-h test period. Expressed as stimulated level/control level ratios, glucocorticoid (cortisol + corticosterone) responses to IGF I after 4 days' culture (2.41 ± 0.20 (SEM) <em>n</em> = 9) were similar to those obtained with ACTH (2.59 ± 0.18, <em>n</em> = 9). A combination of the two peptides had a synergistic effect (5.95 ± 0.79, <em>n</em> = 5).</p><p>The cortisol/corticosterone ratio increased in the presence of IGF I from 1 ± 0.19 to 1.76 ± 0.45 (<em>n</em> = 7, <em>P</em> < 0.02), although less so than in the presence of ACTH (5.50 ± 0.98). Moreover, cortisol production was accompanied by adrostenedione production (2.36ng/10<sup>6</sup> cells, <em>n</em> = 3) similar to that induced by ACTH (2.10 ng/10<sup>6</sup> cells, <em>n</em> = 3). These findings together suggest stimulation of 17α-hydroxylase activity. Cell multiplication was unaffected by IGF I. [<sup>3</sup>H]Thymidine incorporation into DNA reached only 193% ± 17 (SEM) (<em>n</em> = 4) of control levels, whereas with ACTH it dropped to 60% ± 5.</p><p>Our findings show that IGF I alone has no mitogenic effect on adrenocortical cells <em>in vitro</em>, but that it is capable of inducing differentiated steroidogenesis.</p></div>","PeriodicalId":17138,"journal":{"name":"Journal of steroid biochemistry","volume":"36 6","pages":"Pages 583-588"},"PeriodicalIF":0.0000,"publicationDate":"1990-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0022-4731(90)90176-S","citationCount":"13","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of steroid biochemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/002247319090176S","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 13
Abstract
The effects of a physiological dose of IGF I (40 ng/ml ≈ 5 × 10−9 M) on steroidogenesis were studied in bovine adrenal fasciculata cells cultured in serum-free McCoy's medium. They were compared with those of a single dose of ACTH (0.25 ng/ml ≈ 10−10 M) at approximately the concentration inducing half-maximal stimulation. With IGF I, steroidogenesis commenced after 48 h culture and progressively increased throughout the 96-h test period. Expressed as stimulated level/control level ratios, glucocorticoid (cortisol + corticosterone) responses to IGF I after 4 days' culture (2.41 ± 0.20 (SEM) n = 9) were similar to those obtained with ACTH (2.59 ± 0.18, n = 9). A combination of the two peptides had a synergistic effect (5.95 ± 0.79, n = 5).
The cortisol/corticosterone ratio increased in the presence of IGF I from 1 ± 0.19 to 1.76 ± 0.45 (n = 7, P < 0.02), although less so than in the presence of ACTH (5.50 ± 0.98). Moreover, cortisol production was accompanied by adrostenedione production (2.36ng/106 cells, n = 3) similar to that induced by ACTH (2.10 ng/106 cells, n = 3). These findings together suggest stimulation of 17α-hydroxylase activity. Cell multiplication was unaffected by IGF I. [3H]Thymidine incorporation into DNA reached only 193% ± 17 (SEM) (n = 4) of control levels, whereas with ACTH it dropped to 60% ± 5.
Our findings show that IGF I alone has no mitogenic effect on adrenocortical cells in vitro, but that it is capable of inducing differentiated steroidogenesis.