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Progesterone synthesized by Schwann cells during myelin formation regulates neuronal gene expression.
- Source :
-
Molecular biology of the cell [Mol Biol Cell] 2000 Jul; Vol. 11 (7), pp. 2283-95. - Publication Year :
- 2000
-
Abstract
- Previously, progesterone was found to regulate the initiation and biosynthetic rate of myelin synthesis in Schwann cell/neuronal cocultures. The mRNA for cytochrome P450scc (converts cholesterol to pregnenolone), 3beta-hydroxysteroid dehydrogenase (3beta-HSD, converts pregnenolone to progesterone), and the progesterone receptor were found to be markedly induced during active myelin synthesis. However, the cells in the cocultures responsible for these changes were not identified. In this study, in situ hybridization was used to determine the localization of the enzymes responsible for steroid biosynthesis. The mRNA for cytochrome P450scc and 3beta-HSD were detected only in actively myelinating cocultures and were localized exclusively in the Schwann cells. Using immunocytochemistry, with minimal staining of the Schwann cells, we found the progesterone receptor in the dorsal root ganglia (DRG) neurons. The progesterone receptor in the neurons translocated into the nuclei of these cells when progesterone was added to neuronal cultures or during myelin synthesis in the cocultures. Additionally, a marked induction of the progesterone receptor was found in neuronal cultures after the addition of progesterone. The induction of various genes in the neurons was also investigated using mRNA differential display PCR in an attempt to elucidate the mechanism of steroid action on myelin synthesis. Two novel genes were induced in neuronal cultures by progesterone. These genes, along with the progesterone receptor, were also induced in cocultures during myelin synthesis, and their induction was blocked by RU-486 (a progesterone receptor antagonist). These genes were not induced in Schwann cells cultured alone after the addition of progesterone. These results suggest that progesterone is synthesized in Schwann cells and that it can indirectly regulate myelin formation by activating transcription via the classical steroid receptor in the DRG neurons.
- Subjects :
- 3-Hydroxysteroid Dehydrogenases biosynthesis
3-Hydroxysteroid Dehydrogenases genetics
Animals
Cholesterol Side-Chain Cleavage Enzyme biosynthesis
Cholesterol Side-Chain Cleavage Enzyme genetics
Coculture Techniques
Enzyme Induction
Ganglia, Spinal cytology
Ganglia, Spinal metabolism
Immunohistochemistry methods
In Situ Hybridization methods
Myelin Basic Protein genetics
Neurons cytology
Neurons drug effects
Progesterone pharmacology
RNA, Messenger
Rats
Rats, Sprague-Dawley
Receptors, Progesterone biosynthesis
Receptors, Progesterone genetics
Ribosomal Proteins genetics
Schwann Cells cytology
Schwann Cells drug effects
Gene Expression Regulation drug effects
Myelin Sheath metabolism
Neurons metabolism
Progesterone biosynthesis
Schwann Cells metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1059-1524
- Volume :
- 11
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Molecular biology of the cell
- Publication Type :
- Academic Journal
- Accession number :
- 10888668
- Full Text :
- https://doi.org/10.1091/mbc.11.7.2283