| Literature DB >> 3021441 |
J Schwartz, N Billestrup, M Perrin, J Rivier, W Vale.
Abstract
A fluorescein-conjugated bioactive analog of corticotropin-releasing factor (CRF) was synthesized and used to label cells that have high affinity CRF-binding sites. Of cultured bovine anterior pituitary cells, 6.1 +/- 0.6% were visible by fluorescence microscopy after incubation with the analog. Fluorescence was eliminated by coincubation with a 200-fold excess of unlabeled CRF. Treatment with dexamethasone (10(-9)-10(-7) M) decreased visible fluorescence in a dose-dependent manner. These results demonstrate the utility of a fluorescent CRF analog for identification of cells with specific CRF-binding sites and suggest that binding of CRF to anterior pituitary cells is altered by glucocorticoids.Entities:
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Year: 1986 PMID: 3021441 DOI: 10.1210/endo-119-5-2376
Source DB: PubMed Journal: Endocrinology ISSN: 0013-7227 Impact factor: 4.736