First Evidence of Mineralocorticoid Receptor Gene and Protein Expression in Rat and Human Thyroid Tissues and Cell Cultures.
Jacopo MansoMaria Chiara PedronAlberto MondinSimona CensiGianmaria PennelliFrancesca GaluppiniSusi BarolloLoris BertazzaClaudia Maria RaduFrancesca GhiniPaolo SimioniChiara SabbadinFilippo CeccatoDecio ArmaniniCaterina MianPublished in: International journal of molecular sciences (2024)
Aldosterone (Aldo) exerts its action through binding with the mineralocorticoid receptor (MR). Clinically, a link between primary aldosteronism (PA) and thyroid diseases has been hypothesised. However, the presence and activity of MR on the thyroid have not yet been demonstrated. We investigated the gene/protein expression and activation of MR in primary thyroid cell cultures (normal rat thyroid [FRTL-5] and human papillary thyroid cancer [PTC] cell lines, BCPAP and K1) through qRT-PCR analysis, immunofluorescence, and confocal microscopy. We also studied the effects of Aldo on thyroid-specific and inflammation genes in vitro. Paired human normal and neoplastic thyroid tissues were also studied. We demonstrated both gene and protein expression and activation of MR in normal rat thyroid and human PTC lines. Incubation with Aldo induced an acute increase in IL-6 expression in both the FRTL-5 and BCPAP lines, which was antagonised by spironolactone, and an acute and late upregulation of thyroid-specific genes in FRTL-5. MR was also expressed at both gene and protein levels in normal human thyroid tissues and in PTC, with a progressive decline during neoplastic tumourigenesis, particularly in more aggressive histotypes. We present the first evidence of MR gene and protein expression in both normal and pathological thyroid cells and tissues. We have shown that MR is present and functionally activated in thyroid tissue. Binding of Aldo to MR induces the expression of inflammatory and thyroid-specific genes, and the thyroid may thus be considered a novel mineralocorticoid target tissue.
Keyphrases
- endothelial cells
- genome wide
- oxidative stress
- magnetic resonance
- gene expression
- genome wide identification
- poor prognosis
- contrast enhanced
- induced pluripotent stem cells
- copy number
- magnetic resonance imaging
- genome wide analysis
- cell proliferation
- small molecule
- high resolution
- transcription factor
- stem cells
- bone marrow
- high glucose
- angiotensin ii
- cell therapy
- liver failure
- mesenchymal stem cells
- long non coding rna
- hepatitis b virus
- mass spectrometry
- pluripotent stem cells
- extracorporeal membrane oxygenation
- data analysis
- cell cycle arrest
- protein protein