The relationship between growth hormone (GH) messenger ribonucleic acid levels and hormone release from individual cells derived from human GH-secreting pituitary adenomas
- PMID: 2004472
- DOI: 10.1111/j.1365-2265.1991.tb01728.x
The relationship between growth hormone (GH) messenger ribonucleic acid levels and hormone release from individual cells derived from human GH-secreting pituitary adenomas
Abstract
GH mRNA expression and GH release by individual cells derived from four GH-secreting pituitary adenomas were studied by in-situ hybridization and the reverse haemolytic plaque assay, respectively. In addition the percentage of PRL mRNA-containing cells was determined in these cell suspensions. The percentages of GH mRNA-containing cells varied between 52 and 89 while the percentages of GH plaque forming cells varied between 25 and 77. Frequency distributions of GH mRNA levels in individual cells and of individual GH plaque areas showed a majority of the cells having low GH mRNA levels and secreting low amounts of GH respectively, while there is a low proportion of cells expressing high GH mRNA levels and forming large GH plaques. There was a significant correlation between the GH mRNA levels and the GH plaque areas of individual cells from the four adenomas (P less than 0.001). The percentages of PRL mRNA-containing cells in the four different adenomas amounted to less than 1, 5, 2 and 18. Cultured cells from the adenomas consisting of 5 and 18% PRL mRNA-containing cells also contained and released measurable amounts of PRL. Our data show that individual cells from GH-secreting pituitary adenomas are heterogeneous with respect to GH mRNA expression, a small proportion of the cells expressing a high amount of GH mRNA. The heterogeneity in GH mRNA expression is correlated with the heterogeneity in GH release. These observations suggest that a considerable part of GH secreted from a GH-secreting pituitary adenoma is produced by a minority of the GH-secreting tumour cell population.(ABSTRACT TRUNCATED AT 250 WORDS)
Comment in
-
Heterogeneity of growth hormone production in human pituitary tumour cells.Clin Endocrinol (Oxf). 1991 Jan;34(1):3-4. doi: 10.1111/j.1365-2265.1991.tb01727.x. Clin Endocrinol (Oxf). 1991. PMID: 2004470 Review. No abstract available.
Similar articles
-
Long-term in-vitro treatment of human growth hormone (GH)-secreting pituitary adenoma cells with octreotide causes accumulation of intracellular GH and GH mRNA levels.Clin Endocrinol (Oxf). 1992 Sep;37(3):240-8. doi: 10.1111/j.1365-2265.1992.tb02317.x. Clin Endocrinol (Oxf). 1992. PMID: 1424206
-
Detection of growth hormone, prolactin and human beta-chorionic gonadotropin mRNA in growth hormone-secreting pituitary adenomas and in prolactin-secreting pituitary adenomas by in situ hybridization using a non-isotopic detection method.Acta Endocrinol (Copenh). 1993 May;128(5):411-7. doi: 10.1530/acta.0.1280411. Acta Endocrinol (Copenh). 1993. PMID: 8317187
-
A case of pituitary somatotroph adenoma with concomitant secretion of growth hormone, prolactin, and adrenocorticotropic hormone--an adenoma derived from primordial stem cell, studied by immunohistochemistry, in situ hybridization, and cell culture.Acta Neurochir (Wien). 1996;138(8):1002-7. doi: 10.1007/BF01411291. Acta Neurochir (Wien). 1996. PMID: 8890999
-
Heterogeneity of growth hormone production in human pituitary tumour cells.Clin Endocrinol (Oxf). 1991 Jan;34(1):3-4. doi: 10.1111/j.1365-2265.1991.tb01727.x. Clin Endocrinol (Oxf). 1991. PMID: 2004470 Review. No abstract available.
-
[Molecular basis of pituitary adenomas with emphasis on somatotropinomas].Arq Bras Endocrinol Metabol. 2004 Aug;48(4):464-79. doi: 10.1590/s0004-27302004000400006. Epub 2005 Mar 7. Arq Bras Endocrinol Metabol. 2004. PMID: 15761509 Review. Portuguese.
Cited by
-
Structure-function correlations of growth hormone or/and prolactin-producing pituitary adenomas: an in vitro study with the reverse hemolytic plaque assay.J Endocrinol Invest. 1999 Oct;22(9):671-80. doi: 10.1007/BF03343628. J Endocrinol Invest. 1999. PMID: 10595830
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical