The cAMP-Dependent induction of LH receptors in primary cultures of porcine granulosa cells is not due to the expression of an intracellular pool of LH receptors
- PMID: 6307657
- DOI: 10.1210/endo-113-2-825
The cAMP-Dependent induction of LH receptors in primary cultures of porcine granulosa cells is not due to the expression of an intracellular pool of LH receptors
Abstract
The present studies examined whether the increase in cell surface LH receptors in primary cultures of porcine granulosa cells after exposure to FSH or cholera toxin, agents that increase intracellular cAMP, is due to de novo synthesis of the receptor or to a cAMP-dependent translocation of an intracellular pool of LH receptors to the cell surface. LH receptor induction by FSH was fully inhibited by the addition of cycloheximide to the incubation media, but resumed after cycloheximide was removed. These data suggest that FSH-induced LH receptor appearance requires protein synthesis. However, to be confident that the inhibition of LH receptor appearance did not result from lack of transit of preformed receptors requiring a rapidly turning over pool of proteins, we assayed for possible latent receptors in the cell interior by extracting granulosa cells with Triton X-100. Under conditions which detected about 74% of LH receptors in cells exposed to cholera toxin, little [125]iodo-hCG-binding activity was detected in cells not exposed to a cAMP-promoting stimulus. These findings suggest that a preformed pool of LH receptors does not exist in untreated cells, and that the cAMP-mediated induction of LH receptors requires de novo synthesis of the receptor.
Similar articles
-
Developmental coordination of luteinizing hormone/human chorionic gonadotropin (hCG) receptors and acute hCG responsiveness in cultured and freshly harvested porcine granulosa cells.Endocrinology. 1984 Jan;114(1):153-63. doi: 10.1210/endo-114-1-153. Endocrinology. 1984. PMID: 6317341
-
Follicle-stimulating hormone induction of luteinizing hormone receptor in cultured rat granulosa cells: an examination of the need for steroids in the induction process.Endocrinology. 1981 Apr;108(4):1379-85. doi: 10.1210/endo-108-4-1379. Endocrinology. 1981. PMID: 6258904
-
Effect of prolactin on the expression of luteinizing hormone receptors during cell differentiation in cultured rat granulosa cells.Endocrinology. 1999 Aug;140(8):3444-51. doi: 10.1210/endo.140.8.6888. Endocrinology. 1999. PMID: 10433199
-
Enhanced follicle-stimulating hormone activity of deglycosylated human chorionic gonadotropin in ovarian granulosa cells.Endocrinology. 1985 Jan;116(1):59-64. doi: 10.1210/endo-116-1-59. Endocrinology. 1985. PMID: 2981077
-
Androgen inhibition of follicle-stimulating hormone-stimulated luteinizing hormone receptor formation in cultured rat granulosa cells.Endocrinology. 1985 Jul;117(1):13-22. doi: 10.1210/endo-117-1-13. Endocrinology. 1985. PMID: 2988911
Cited by
-
Recent Insight on the Non-coding RNAs in Mesenchymal Stem Cell-Derived Exosomes: Regulatory and Therapeutic Role in Regenerative Medicine and Tissue Engineering.Front Cardiovasc Med. 2021 Oct 1;8:737512. doi: 10.3389/fcvm.2021.737512. eCollection 2021. Front Cardiovasc Med. 2021. PMID: 34660740 Free PMC article. Review.
-
A Comparative Analysis of Multipotent Mesenchymal Stromal Cells derived from Different Sources, with a Focus on Neuroregenerative Potential.Sci Rep. 2020 Mar 9;10(1):4290. doi: 10.1038/s41598-020-61167-z. Sci Rep. 2020. PMID: 32152403 Free PMC article.
-
Luteinizing hormone receptor appearance in cultured porcine granulosa cells requires continual presence of follicle-stimulating hormone.Proc Natl Acad Sci U S A. 1983 Sep;80(18):5631-5. doi: 10.1073/pnas.80.18.5631. Proc Natl Acad Sci U S A. 1983. PMID: 6310585 Free PMC article.
-
Induction of lutropin receptors by lutropin and cyclic AMP in cultured mouse tumour (MA10) Leydig cells.Biochem J. 1990 Sep 1;270(2):499-503. doi: 10.1042/bj2700499. Biochem J. 1990. PMID: 2169244 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
