| Autor: |
Watson CS; Department of Human Biological Chemistry and Genetics, University of Texas Medical Branch, Galveston 77555-0645, USA., Norfleet AM, Pappas TC, Gametchu B |
| Jazyk: |
angličtina |
| Zdroj: |
Steroids [Steroids] 1999 Jan-Feb; Vol. 64 (1-2), pp. 5-13. |
| DOI: |
10.1016/s0039-128x(98)00107-x |
| Abstrakt: |
The focus of our work on rapid actions of estrogens has been on the immuno-identification of a membrane version of the estrogen receptor-alpha (mERalpha) and the correlation of the presence of this receptor to the rapid secretion of prolactin in pituitary tumor cells. We demonstrated the mERalpha by both fluorescence and immuno-enzyme-cytochemistry and with both conventional and confocal microscopy in the cell line GH3/B6 and its sublines. Its presence on cells (including recently subcloned ones) is very heterogenous, unlike the nuclear ERalpha, which is present in every cell. An impeded ligand (estradiol covalently linked to BSA) binds to mERalpha and elicits the same response. A total of eight antibodies to ERalpha recognize mERalpha, making it likely that the membrane and nuclear proteins are highly related. Immuno-identification techniques have also been used to identify mERalpha on the MCF-7 human breast cancer cell line. Estradiol at very low concentrations elicits prolactin release from GH3/B6 cells within a few minutes of application. This response is bimodal, with effective concentrations in both the picomolar and nanomolar ranges. Prolactin release is also elicited or inhibited by ERalpha-specific antibodies. The characteristics of mERalpha and the membrane receptor for glucocorticoids have many similarities, suggesting that this mode of subcellular location/function alternative might be used by other members of the gene family. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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