Department of Cell & Molecular Biology, Karolinska Institute, von Eulers väg 3, 17177 Stockholm, Sweden.
Heart Fail Rev. 2010 Mar;15(2):111-5. doi: 10.1007/s10741-008-9119-5. Epub 2008 Nov 14.
Many patients have been characterized harboring a mutation in thyroid hormone receptor (TR) beta. Surprisingly none has yet been identified carrying a mutation in TRalpha1. To facilitate the identification of such patients, several animal models with a mutant TRalpha1 have been generated. While some phenotypic characteristics, such as an adult euthyroidism, are similar in the mutant mice, other aspects such as metabolism are quite variable. This review summarizes the most important consequences of a mutation in TRalpha1 in mice focusing on the TRalpha1-R384C mutation, and projects the insights from the animal models to a putative phenotype of patients with a mutated TRalpha1.
许多患者被描述为甲状腺激素受体 (TR)β 突变携带者。令人惊讶的是,尚未发现 TRα1 突变携带者。为了方便此类患者的鉴定,已经生成了几种具有突变 TRα1 的动物模型。虽然一些表型特征,如成年甲状腺功能正常,在突变小鼠中相似,但其他方面,如代谢,变化很大。本文综述了小鼠中 TRα1 突变的最重要后果,重点介绍了 TRα1-R384C 突变,并将动物模型的见解投射到突变 TRα1 患者的假定表型上。