Glucocorticoid receptor identified on nuclear envelopes of male rat livers by affinity labeling and immunochemistry

Gilian M. Howell, Jan Åke Gustafsson, Yvonne A. Lefebvre

    Research output: Contribution to journalArticlepeer-review

    19 Scopus citations

    Abstract

    To exert their action at the genome, steroids must traverse the nuclear envelope, either alone or complexed to their receptor. Our previous studies identified two classes of dexamethasone-binding sites on male rat liver nuclear envelopes: a low capacity, high affinity site and a high capacity, low affinity site. The affinity reagent, [3H]dexarnethasone mesylate, labeled peptides at 35-85 kDa, which may be the low affinity glucocorticoid-binding peptides, as these peptides showed the same response to hormonal manipulation as the low affinity [3H] dexamethasone-binding sites previously characterized. With dexamethasone mesylate and a monoclonal antibody against the glucorticoid receptor, we have confirmed that the high affinity binding site on the nuclear envelope is the glucocorticoid receptor. Affinity labeling revealed the presence of a doublet of peptides at 85 and 110 kDa, in the same mol wt range as that reported for the glucocorticoid receptor. Furthermore, these affinity-labeled peptides responded to hormonal manipulation like nuclear glucocorticoid receptors. The monoclonal antibody identified a doublet of peptides, a major component of 92-94 kDa and a minor component of 98 kDa. Again, both peptides responded to hormonal manipulation like nuclear glucocorticoid receptors. The nuclear envelope-associated glucocorticoid receptor is not extracted by 0.1 M NaCl or 1% Triton X-100. These results show that glucocorticoid hormone interacts with the nuclear envelope via binding to the transformed glucocorticoid receptor, lending support to the two-step model of steroid hormone action.

    Original languageEnglish (US)
    Pages (from-to)1087-1096
    Number of pages10
    JournalEndocrinology
    Volume127
    Issue number3
    StatePublished - Sep 1990

    ASJC Scopus subject areas

    • Endocrinology

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