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Publication : Complete activation of thyroid hormone receptor β by T3 is essential for normal cochlear function and morphology in mice.

First Author  Richter CP Year  2011
Journal  Cell Physiol Biochem Volume  28
Issue  5 Pages  997-1008
PubMed ID  22178950 Mgi Jnum  J:312622
Mgi Id  MGI:6791978 Doi  10.1159/000335812
Citation  Richter CP, et al. (2011) Complete activation of thyroid hormone receptor beta by T3 is essential for normal cochlear function and morphology in mice. Cell Physiol Biochem 28(5):997-1008
abstractText  BACKGROUND/AIMS: Thyroid hormones (THs) regulate many developmental processes, including the developmental onset of cochlear differentiation and function. TH action is mediated mostly by triiodothyronine (T3) bound to thyroid hormone nuclear receptors (TRs). At positive regulated genes and in the absence of THs, nuclear co-repressors are bound to TRs and decrease basal transcription rate. Ligand (T(3)) binding results in the dissociation of co-repressors and the recruitment of co-activators to the complex, which results in full transcriptional activation. METHODS: We measured cochlear function in two knock-in mouse models: TRbeta(E457A/E457A), with the TRbeta co-activator binding surface (AF-2) disrupted to prevent co-activator binding; and TRbeta(Delta337T/Delta337T), which is unable to bind T(3). Cochlear morphology and function were analyzed in 10-week-old normal and mutated mice. Cochlear function was determined by measuring auditory brainstem responses, cochlear tuning and compound action potential (CAP) thresholds. RESULTS: All TRbeta(Delta337T/Delta337T) and 85% of the TRbeta(E457A/E457A) mice presented elevated CAP thresholds (P < 0.05 or less). Five percent of the TRbeta(E457A/E457A) mice presented normal CAP thresholds with broadened cochlear tuning. TRbeta(E457A/E457A) and TRbeta(Delta337T/Delta337T) presented developmental defects that led to a decreased width (P < 0.01) and an increased thickness (P<0.01) of the tectorial membrane. In addition, TRbeta(Delta337T/Delta337T) animals showed an increased tectorial membrane area (P<0.01). CONCLUSION: Both mutations were deleterious to tectorial membrane development and led to important alterations in cochlear morphology and loss of cochlear function.
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