Publications

Latest publication 09/13/2020

Generation and Characterization of a New Resistance to Thyroid Hormone Mouse Mod

Background In humans, Resistance to Thyroid Hormone (RTH) caused by mutations in the thyroid hormone receptor alpha (THRA) gene, RTHalpha,...

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    [title] => Generation and Characterization of a New Resistance to Thyroid Hormone Mouse Mod
    [paragraph] => Generation and Characterization of a New Resistance to Thyroid Hormone Mouse Model with Thyroid Hormone Receptor Alpha Gene Mutation
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Authors
Y Liang, D Zhao, R Wang et al

 Lab
The First Affiliated Hospital of China Medical University, Liaoning, China;
Journal
Thyroid
Abstract
Background In humans, Resistance to Thyroid Hormone (RTH) caused by mutations in the thyroid hormone receptor alpha (THRA) gene, RTHalpha, manifests as tissue-specific hypothyroidism and circulating thyroid hormone levels that exhibits hypothyroid-like clinical features. Before the identification of patients with RTHalpha, several Thralpha1 knock-in mouse models were generated to clarify the function of TRalpha1. However, the phenotypes of these mice were not consistent with the clinical presentation of RTHalpha in humans. For the present study we generated a RTHalpha mouse model that carries the Thra1 E403X mutation found in human RTHalpha patients. Here we report the gross phenotypes of this mouse RTH_ model. Methods Traditional homologous recombination gene targeting techniques were used to introduce a mutation (Thralpha1 E403X) in the mouse Thra gene. The phenotypes of the resulting mice were studied and compared to clinical features seen for RTH_ with THRAE403X. Results Thralpha1E403X/E403X homozygous mice exhibited severe neurological phenotypes, such as spasticity and motor ataxia, which were similar to those observed in endemic cretinism. Thralpha1E403X/+ heterozygous mice reproduced most clinical manifestations of the patient with RTHalpha, such as a normal survival rate and male fertility, as well as delayed postnatal growth and development, neurological and motor coordination deficits, and anemia. The mice had typical thyroid function with a modest increase in serum T3 levels, a low of T4/T3 ratio, and low rT3 levels. Conclusions The Thralpha1E403X/+ mice faithfully recapitulate clinical features of human RTHalpha, and thus can provide a useful tool to dissect the role of TRalpha1 in development and to determine the pathological mechanisms of RTHalpha.
BIOSEB Instruments Used
Grip strength test (BIO-GS3)
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An easy way to objectively quantify the muscular strength of mice and rats, and to assess the effect of drugs, toxins, muscular (i.e. myopathy) and neurodegenerative diseases on muscular degeneration. It is widely used in conjunction with the ROTAROD motor coordination test: a normally coordinated rodent will show a decreased latency to fall off the rotating rod if its muscular strength is low. The Grip Strength Test is a must for your research on activity, motor control & coordination, and is particularly well suited for studies on Parkinson's & Huntington's disease.
New features GS4 - 2023: Color display with permanent backlight screen for easier reading, reset by footswitch, Improved battery time, Larger data memory of 500 values, Animal counter, USB port (charging/data transfer)

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