Genistein‐mediated thermogenesis and white‐to‐beige adipocyte differentiation involve transcriptional activation of cAMP response elements in the Ucp1 promoter

• Published in: The FASEB journal Vol. 37; no. 8; pp. e23079 - n/a
• Main Authors: Fuentes‐Romero, Rebeca, Velázquez‐Villegas, Laura A., Vasquez‐Reyes, Sarai, Pérez‐Jiménez, Berenice, Domínguez Velázquez, Zuleima N., Sánchez‐Tapia, Mónica, Vargas‐Castillo, Ariana, Tobón‐Cornejo, Sandra, López‐Barradas, Adriana M., Mendoza, Valentín, Torres, Nimbe, López‐Casillas, Fernando, Tovar, Armando R.
• Format: Journal Article
• Language: English
• Published: United States 01-08-2023
• Subjects: Adipocytes, Beige - metabolism; Adipose Tissue, Brown - metabolism; Adipose Tissue, White - metabolism; Animals; Genistein - pharmacology; Mice; Rats; Response Elements; Thermogenesis - genetics; Transcriptional Activation; Uncoupling Protein 1 - genetics; Uncoupling Protein 1 - metabolism
• ISSN: 0892-6638; 1530-6860
• DOI: 10.1096/fj.202300139RR

Genistein is an isoflavone present in soybeans and is considered a bioactive compound due to its widely reported biological activity. We have previously shown that intraperitoneal genistein administration and diet supplementation activates the thermogenic program in rats and mice subcutaneous white adipose tissue (scWAT) under multiple environmental cues, including cold exposure and high‐fat diet feeding. However, the mechanistic insights of this process were not previously unveiled. Uncoupling protein 1 (UCP1), a mitochondrial membrane polypeptide responsible for dissipating energy into heat, is considered the most relevant thermogenic marker; thus, we aimed to evaluate whether genistein regulates UCP1 transcription. Here we show that genistein administration to thermoneutral‐housed mice leads to the appearance of beige adipocyte markers, including a sharp upregulation of UCP1 expression and protein abundance in scWAT. Reporter assays showed an increase in UCP1 promoter activity after genistein stimulation, and in silico analysis revealed the presence of estrogen (ERE) and cAMP (CRE) response elements as putative candidates of genistein activation. Mutation of the CRE but not the ERE reduced genistein‐induced promoter activity by 51%. Additionally, in vitro and in vivo ChIP assays demonstrated the binding of CREB to the UCP1 promoter after acute genistein administration. Taken together, these data elucidate the mechanism of genistein‐mediated UCP1 induction and confirm its potential applications in managing metabolic disorders.
Genistein induces the thermogenic program in white adipose tissue via cAMP/PKA/CREB pathway to promote Ucp1 transcription. This mechanism of beige remodeling is independent of sympathetic nervous system activation.