Gene expression of T3-regulated genes in a mouse model of the human thyroid hormone resistance

L. A. Santiago, L. C. Faustino, G. F. Pereira, G. E. Imperio, C. C. Pazos-Moura, F. E. Wondisford, F. F. Bloise, T. M. Ortiga-Carvalho

Research output: Contribution to journalArticlepeer-review

Abstract

Aims To understand how thyroid hormone (TH) regulates tissue-specific gene expression in patients with the syndrome of resistance to TH (RTHβ), we used a mouse model that replicates the human RTHβ, specifically the ∆ 337T mutation in the thyroid hormone receptor β (THRβ). Main methods We investigated the expression of key TH target genes in the pituitary and liver of TRβ∆ 337T and wild type THRβ mice by qPCR before and after a T3 suppression test consisting of the administration of increasing concentrations of T3 to hypothyroid mice. Key findings Pituitary Tshb and Cga expression decreased and Gh expression increased in TRβ∆ 337T mice after T3 suppression. The stimulation of positively regulated TH genes was heterogeneous in the liver. Levels of liver Me1 and Thsrp were elevated in TRβ∆ 337T mice after T3 administration. Slc16a2 and Gpd2 did not respond to T3 stimulation in the liver of TRβ∆ 337T mice whereas Dio1 response was lower than that observed in WT mice. Moreover, although Chdh and Upd1 genes were negatively regulated in the liver, the expression of these genes was elevated after T3 suppression. We did not observe significant changes in THRα expression in the liver and pituitary, while THRβ levels were diminished in the pituitary and increased in the liver. Significance Using a model expressing a THRβ unable to bind T3, we showed the expression pattern of liver negative and positive regulated genes by T3.

Original languageEnglish (US)
Pages (from-to)93-99
Number of pages7
JournalLife Sciences
Volume170
DOIs
StatePublished - Feb 1 2017
Externally publishedYes

Keywords

  • Gene expression
  • Liver
  • Thyroid hormone receptor

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Pharmacology, Toxicology and Pharmaceutics(all)

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