Autoradiographic localization of 3H-glucocorticoids and 3H-cortexolone in mouse pituitary

• Published in: Cell and tissue research 1979-08, Vol.200 (2), p.311-322
• Main Authors: Coutard, M, Osborne-Pellegrin, M J, Funder, J
• Format: Article
• Language: English
• Subjects: 17-Hydroxycorticosteroids - metabolism; Animals; Autoradiography; Cell Nucleus - metabolism; Corticosterone - metabolism; Cortodoxone - metabolism; Cytoplasm - metabolism; Dexamethasone - metabolism; Female; Mice; Pituitary Gland - metabolism; Pituitary Gland, Anterior - metabolism; Pituitary Gland, Posterior - metabolism
• ISSN: 0302-766X; 1432-0878
• DOI: 10.1007/BF00236423

Autoradiograms of mouse pituitaries were prepared 30 min after injection of 3H-dexamethasone (3HDM), 3H-corticosterone (3HB) and 3H-cortexolone (3HS) either alone or in the presence of competing unlabelled steroids. 3H-dexamethasone accumulated in cell nuclei of both the pars distalis and the pars nervosa but not in those of the pars intermedia. This preferential accumulation (nuclear/cytoplasmic grain density, 4 : 1) was abolished by the concurrent administration of excess dexamethasone. 3H-corticosterone, to a much less marked extent than 3H-dexamethasone, accumulated in cell nuclei of the pars distalis but not in those of the pars intermedia and the pars nervosa. Excess unlabelled corticosterone diminished nuclear grain density in the pars distalis. After 3-h-cortexolone injection, preferential nuclear uptake was not observed. In a second series of experiments, excess dexamethasone (10 x, 100 x), corticosterone (100 x, 300 x) and cortexolone (100 x, 300 x) administered with 3H-dexamethasone were without effect on cytoplasmic grain density but totally abolished preferential nuclear accumulation. Parallel biochemical studies on kidney cytoplasmic preparations from the same animals showed no differences in total cytoplasmic radioactivity between treatments but marked differences in cytoplasmic bound 3H-dexamethasone. The results demonstrate: i) that dexamethasone binds specifically to cell nuclei of the pars distalis and the pars nervosa and that this nuclear concentration is abolished by competing corticosterone and cortexolone as well as dexamethasone; ii) that corticosterone localizes in cell nuclei of the pars distalis but much less markedly than dexamethasone; iii) that cortexolone fullfils the criteria of a glucocorticoid antagonist at the pituitary cell level.