The impact of mineralocorticoid and glucocorticoid receptor interaction on corticosteroid transcriptional outcomes

• Published in: Molecular and cellular endocrinology 2024-12, Vol.594, p.112389, Article 112389
• Main Authors: Alvarez de la Rosa, Diego, Ramos-Hernández, Zuleima, Weller-Pérez, Julián, Johnson, Thomas A., Hager, Gordon L.
• Format: Article
• Language: English
• Subjects: Adrenal Cortex Hormones - metabolism; Aldosterone; Animals; brain; corticosterone; cortisol; electrolytes; gene expression; Gene Expression Regulation - drug effects; glucocorticoid receptors; Glucocorticoids; Glucocorticoids - metabolism; Glucocorticoids - pharmacology; Heteromerization; homeostasis; Humans; immunomodulation; ligands; metabolism; Nuclear receptor; Protein Binding; Protein Multimerization; Receptors, Glucocorticoid - genetics; Receptors, Glucocorticoid - metabolism; Receptors, Mineralocorticoid - genetics; Receptors, Mineralocorticoid - metabolism; Signal Transduction; Steroid hormone; subfamily; transcription (genetics); Transcription, Genetic - drug effects
• ISSN: 0303-7207; 1872-8057; 1872-8057
• DOI: 10.1016/j.mce.2024.112389

The mineralocorticoid and glucocorticoid receptors (MR and GR, respectively) are members of the steroid receptor subfamily of nuclear receptors. Their main function is to act as ligand-activated transcription factors, transducing the effects of corticosteroid hormones (aldosterone and glucocorticoids) by modulating gene expression. Corticosteroid signaling is essential for homeostasis and adaptation to different forms of stress. GR responds to glucocorticoids by regulating genes involved in development, metabolism, immunomodulation and brain function. MR is best known for mediating the effects of aldosterone, a key hormone controlling electrolyte and water homeostasis. In addition to aldosterone, MR binds glucocorticoids (cortisol and corticosterone) with equally high affinity. This ligand promiscuity has important repercussions to understand MR function, as well as glucocorticoid signaling. MR and GR share significant sequence and structural similarities, regulate overlapping sets of genes and are able to interact forming heteromeric complexes. However, the precise role of these heteromers in regulating corticosteroid-regulated transcriptional outcomes remains an open question. In this review, we examine the evidence supporting MR-GR heteromerization, the molecular determinants of complex formation and their possible role in differential regulation of transcription in different cellular contexts and ligand availability.