Abstract
We recently demonstrated that transformed murine Leydig cells (MA-10) responded to endothelin-1 (ET-1) via increased steroidogenesis. This study addresses the endothelin receptor subtype present on this cell line and whether or not the cells produce ET-1. The expression of the preproendothelin-1 (PPET-1) gene was investigated by Northern blot analysis, and PPET-1 mRNA was found to be <0.2% of that present in pulmonary endothelial cells. The medium from MA-10 cells, maintained under serum-free conditions, was analyzed by radio-immunoassay to determine immunoreactive-ET-1 production and ET-1 levels were found to be below the sensitivity of the assay (<10 pg/ml). The data from competitive binding experiments with [125I]ET-1 and unlabeled ET-1, ET-3 and receptor subtype selective ligands yielded a single class of high affinity binding sites with ETA receptor subtype characteristics. The results of this study demonstrate that MA-10 cells possess the ETA receptor subtype but do not produce significant quantities of ET-1 under basal conditions.
Original language | English (US) |
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Pages (from-to) | 91-96 |
Number of pages | 6 |
Journal | Molecular and Cellular Biochemistry |
Volume | 136 |
Issue number | 1 |
DOIs | |
State | Published - Jul 1994 |
Externally published | Yes |
Keywords
- Leydig tumor cells
- endothelin receptor
- endothelin-1
ASJC Scopus subject areas
- Molecular Biology
- Clinical Biochemistry
- Cell Biology