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J. Biol. Chem., Vol. 259, Issue 2, 1186-1195, 01, 1984
CP Bastl, CA Barnett, TJ Schmidt and G Litwack
Studies with RU26988, a synthetic glucocorticoid which does not bind to
aldosterone receptors, suggest glucocorticoid-induced colonic cation
transport is affected through glucocorticoid-specific receptors. RU26988
produced a 700% increase in sodium absorption and doubled transmural
potential difference in proximal and distal colon of adrenalectomized rats.
Scatchard analysis suggested a single class of receptors with a KD of
approximately 10(-9) M. Competition of unlabeled steroids for
[3H]triamcinolone acetonide-binding sites paralleled the steroids' biologic
potency as glucocorticoids. Heat treatment (25 degrees C, 30 min) markedly
enhanced binding of the glucocorticoid- receptor complexes to
DNA-cellulose. The activated receptor from both proximal and distal colon
was eluted in the prewash from DEAE-Sephadex A-50 anion exchange columns
both in the presence and absence of protease inhibitors and has an
estimated molecular weight (Stokes radius) of 33,000-37,000 (25-26 A).
These results identify the colonic receptor as glucocorticoid binder IB, a
receptor previously identified as the major binder only in kidney cortex.
The finding of an apparently unique receptor in the two tissues where
glucocorticoids stimulate cation transport suggests that the phenotypic
response mediated by glucocorticoids in different tissues might be
determined by the structure of the receptor and that glucocorticoid binder
IB is the glucocorticoid cation transport receptor.
Glucocorticoid stimulation of sodium absorption in colon epithelia is mediated by corticosteroid IB receptor
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