GH3 cell secretion of growth hormone and prolactin increases spontaneously during perifusion
- PMID: 3667488
- DOI: 10.1007/BF02620981
GH3 cell secretion of growth hormone and prolactin increases spontaneously during perifusion
Abstract
GH3 cell secretory activity was studied in long-term perifusion to define previously reported spontaneous increases in growth hormone (GH) and prolactin production (PRL). Mechanically harvested cells (1 X 10(7)/column) were perifused at 4 ml/h for 72 h. A basal period of variable duration (8 to 12 h), during which hormone secretion was stable, was followed by steadily increasing secretion rates. Changes in cell number were not sufficient to account for increased hormone secretion rates: a) there was no significant change in cell count after 72 h (0.97 +/- 0.03 X 10(7); n = 18); b) mean cell column DNA content increased 25.5% above the base value, whereas GH secretion rose 385% and PRL rose 178% (n = 5). Observed differences in the duration of the basal secretion period, the basal secretory rate, and the magnitude of secretory rate increase were associated with several variables: a) variability within a subline was a function of passage number: GH secretion decreased and PRL secretion increased with subculture number; b) cells with identical lot and freeze numbers, but received at different times, behaved differently; c) the presence of an antifungal agent (nystatin) altered hormone secretion reproducibly.
Conclusions: a) rates of GH and PRL secretion rise spontaneously in perifusion without a proportional increase in GH3 cell number; b) fluctuations in the rate of GH3 cell secretion of GH and PRL are not entirely random but are determined by several definable variables.
Similar articles
-
Deleterious effects of fungizone on growth hormone and prolactin secretion by cultured GH3 cells.In Vitro Cell Dev Biol. 1987 Dec;23(12):837-40. doi: 10.1007/BF02620962. In Vitro Cell Dev Biol. 1987. PMID: 3693251
-
Medium flow rate modulates autocrine-paracrine feedback of GH and PRL release by perifused GH3 cells.In Vitro Cell Dev Biol. 1990 May;26(5):482-92. doi: 10.1007/BF02624090. In Vitro Cell Dev Biol. 1990. PMID: 2351641
-
Autocrine-paracrine inhibition of growth hormone and prolactin production by GH3 cell-conditioned medium.In Vitro Cell Dev Biol. 1989 Jun;25(6):528-34. doi: 10.1007/BF02623565. In Vitro Cell Dev Biol. 1989. PMID: 2661520
-
Epidermal growth factor, insulin, and estrogen stimulate development of prolactin-secreting cells in cultures of GH3 cells.Cell Tissue Res. 2000 Feb;299(2):237-43. doi: 10.1007/s004419900147. Cell Tissue Res. 2000. PMID: 10741464
-
Effect of activin on production and secretion of prolactin and growth hormone in cultured rat GH3 cells.Eur J Endocrinol. 2000 May;142(5):506-11. doi: 10.1530/eje.0.1420506. Eur J Endocrinol. 2000. PMID: 10802530
Cited by
-
Similarities and differences between two modes of antagonism of the thyroid hormone receptor.ACS Chem Biol. 2011 Oct 21;6(10):1096-106. doi: 10.1021/cb200092v. Epub 2011 Aug 15. ACS Chem Biol. 2011. PMID: 21815645 Free PMC article.
-
Deleterious effects of fungizone on growth hormone and prolactin secretion by cultured GH3 cells.In Vitro Cell Dev Biol. 1987 Dec;23(12):837-40. doi: 10.1007/BF02620962. In Vitro Cell Dev Biol. 1987. PMID: 3693251
-
Augmented Growth Hormone Secretion and Stat3 Phosphorylation in an Aryl Hydrocarbon Receptor Interacting Protein (AIP)-Disrupted Somatotroph Cell Line.PLoS One. 2016 Oct 5;11(10):e0164131. doi: 10.1371/journal.pone.0164131. eCollection 2016. PLoS One. 2016. PMID: 27706259 Free PMC article.
-
Medium flow rate modulates autocrine-paracrine feedback of GH and PRL release by perifused GH3 cells.In Vitro Cell Dev Biol. 1990 May;26(5):482-92. doi: 10.1007/BF02624090. In Vitro Cell Dev Biol. 1990. PMID: 2351641
-
Perifusion model system to culture bovine hypothalamic slices in series with dispersed anterior pituitary cells.In Vitro Cell Dev Biol Anim. 1994 Jul;30A(7):435-42. doi: 10.1007/BF02631311. In Vitro Cell Dev Biol Anim. 1994. PMID: 7952512
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Medical