Growth hormone-releasing factor stimulates proliferation of somatotrophs in vitro
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Growth hormone-releasing factor stimulates proliferation of somatotrophs in vitro. / Billestrup, Nils; Swanson, L W; Vale, W.
In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 83, No. 18, 09.1986, p. 6854-7.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Growth hormone-releasing factor stimulates proliferation of somatotrophs in vitro
AU - Billestrup, Nils
AU - Swanson, L W
AU - Vale, W
PY - 1986/9
Y1 - 1986/9
N2 - The mitogenic effect of the hypothalamic peptides growth hormone-releasing factor (GRF) and somatostatin on cultured growth hormone (GH)-producing cells (somatotrophs) was studied. Using autoradiographic detection of [3H]thymidine uptake and immunocytochemical identification of GH-producing cells, we show that 5 nM GRF causes a 20-fold increase in the percentage of somatotrophs labeled with [3H]thymidine. The total number of somatotrophs in GRF-treated cultures was increased by 60%. Somatostatin had no measurable effect on the labeling index by itself, but it partly inhibited the GRF-induced increase in both the labeling index and the total number of cells. Forskolin caused an increase in both the percentage of somatotrophs with a [3H]thymidine-labeled nucleus and the somatotroph number similar to that caused by GRF. GH secretion as well as cellular GH content in the GRF- or forskolin-treated cells increased with culture time over the entire period, whereas secretion and content of GH gradually decreased in control or somatostatin-treated cultures during the entire culture period. These data suggest that GRF and somatostatin regulate the mitotic activity of GH-producing cells and that the effect of GRF is possibly mediated by cyclic AMP.
AB - The mitogenic effect of the hypothalamic peptides growth hormone-releasing factor (GRF) and somatostatin on cultured growth hormone (GH)-producing cells (somatotrophs) was studied. Using autoradiographic detection of [3H]thymidine uptake and immunocytochemical identification of GH-producing cells, we show that 5 nM GRF causes a 20-fold increase in the percentage of somatotrophs labeled with [3H]thymidine. The total number of somatotrophs in GRF-treated cultures was increased by 60%. Somatostatin had no measurable effect on the labeling index by itself, but it partly inhibited the GRF-induced increase in both the labeling index and the total number of cells. Forskolin caused an increase in both the percentage of somatotrophs with a [3H]thymidine-labeled nucleus and the somatotroph number similar to that caused by GRF. GH secretion as well as cellular GH content in the GRF- or forskolin-treated cells increased with culture time over the entire period, whereas secretion and content of GH gradually decreased in control or somatostatin-treated cultures during the entire culture period. These data suggest that GRF and somatostatin regulate the mitotic activity of GH-producing cells and that the effect of GRF is possibly mediated by cyclic AMP.
KW - Animals
KW - Cell Division
KW - Cells, Cultured
KW - Cyclic AMP
KW - Growth Hormone
KW - Growth Hormone-Releasing Hormone
KW - Male
KW - Pituitary Gland, Anterior
KW - Rats
KW - Rats, Inbred Strains
M3 - Journal article
C2 - 3018748
VL - 83
SP - 6854
EP - 6857
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
SN - 0027-8424
IS - 18
ER -
ID: 132900901