Alternative ligands for thyroid hormone receptors

被引:14
作者
Lazcano, Ivan [1 ,2 ]
Hernandez-Puga, Gabriela [2 ]
Pablo Robles, Juan [1 ]
Orozco, Aurea [1 ]
机构
[1] UNAM, Inst Neurobiol, Blvd Juriquilla 3001, Queretaro 76230, Qro, Mexico
[2] Univ Autonoma Queretaro, Fac Med, Dept Invest Biomed, Santiago De Queretaro, Qro, Mexico
关键词
Thyroid hormones; Thyroid hormone receptors; 3,5-T2; TRIAC; Alternative ligand; Thyroid hormone analogs; TYPE-2 IODOTHYRONINE DEIODINASE; ENDOCRINE DISRUPTING CHEMICALS; IN-VIVO ANALYSIS; TRIIODOTHYROACETIC ACID; EQUILIBRIUM DIALYSIS/RADIOIMMUNOASSAY; 3,5,3-TRIIODOTHYROACETIC ACID; PHENOL COMPOUNDS; UNDILUTED SERUM; METABOLIC-RATE; AGONIST GC-1;
D O I
10.1016/j.mce.2019.05.007
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Thyroid hormone receptors (TRs) are ligand-dependent transcription factors that activate or repress gene transcription, resulting in the regulation of numerous physiological programs. While 3,3', 5-L-triiodothyronine is the TR cognate ligand, these receptors can also be activated by various alternative ligands, including endogenous and synthetic molecules capable of inducing diverse active receptor conformations that influence thyroid hormone-dependent signaling pathways. This review mainly discusses current knowledge on 3,5-diiodo-L-thyronine and 3,5,3'-triiodothyroacetic acid, two endogenous molecules that bind to TRs and regulate gene expression; and the molecular interactions between TRs and ligands, like synthetic thyromimetics developed to target specific TR isoforms for tissue-specific regulation of thyroid-related disorders, or endocrine disruptors that have allowed the design of new analogues and revealed essential amino acids for thyroid hormone binding.
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页数:11
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