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The binding of deoxycorticosterone by the AtT-20 cell.
Journal of Steroid Biochemistry
|April 1, 1984
Summary
A novel steroid hormone binding site in AtT-20 cells binds 11-deoxycorticosterone (DOC) but not other steroids. This low-affinity site, located in the particulate fraction, may be part of a hormone-metabolizing system.
Area of Science:
- Endocrinology
- Cell Biology
- Molecular Pharmacology
Background:
- The AtT-20 cell line is a model for studying steroid hormone action.
- Glucocorticoid receptors are well-characterized in these cells.
- The existence of other steroid binding sites is less understood.
Purpose of the Study:
- To characterize a novel steroid hormone binding site in AtT-20 cells.
- To determine the binding specificity and characteristics of this new site.
- To investigate the potential role of this site in hormone action or metabolism.
Main Methods:
- Radioligand binding assays using 11-deoxycorticosterone (DOC).
- Scatchard analysis to assess binding affinity and capacity.
- Cellular fractionation to determine the subcellular localization of the binding site.
- Metabolic studies to investigate steroid transformation.
Main Results:
- A novel binding site in AtT-20 cells was identified that specifically binds 11-deoxycorticosterone (DOC).
- This site does not bind glucocorticoids, estrogens, mineralocorticoids, or progestins.
- Scatchard analysis indicated a high number of sites with low affinity for DOC.
- The binding site is located in the particulate fraction, with some association with nuclei.
- AtT-20 cells metabolize DOC, converting up to 50% into a metabolite.
Conclusions:
- AtT-20 cells possess a unique, low-affinity binding site for 11-deoxycorticosterone (DOC).
- The site's characteristics suggest it is likely involved in hormone metabolism rather than direct hormone action.
- Further research is needed to elucidate the precise function of this DOC-binding system.