An Update on Human Thyroid Hormone Receptors in Health and Disease: Chemistry, Physiology and Pathophysiology

Liaquat Alikhan Sheerinbanu, S. Sharmila, M. M. Aruldhas
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Abstract

Iodothyronines, the tetra- and tri-iodothyronines (T 4 and T 3 ), commonly known as thyroid hormones (THs), are secreted by thyroid glands. Thyroid hormones influence the growth and differentiation of every organ of the body via specific nuclear receptors (TRs), which belong to the nuclear receptor superfamily. Though thyroid glands secrete predominantly T 4 (which remains bound to its serum binding proteins), T 3 is the biologically active TH. Free T 4 enters the target cells through specific transporters and is converted into T 3 by cell-specific isoforms of cytoplasmic 5' deiodinase, which regulate the circulating T 3 levels and its availability for nuclear TRs in a tissue-specific manner. T 3 is then translocated to the nucleus, with the help of NADPH-dependent cytosolic transporter, where it binds to the monomers of TR subtypes (TRα and TRβ). Prior to the binding of T 3 , TR monomer dimerizes with the 9-cis retinoic acid or retinoid X receptor (RXR) and the TR-RXR heterodimer, in association with corepressors, binds to specific TR response element (TRE) in the target genes. Upon T 3 binding to the TR monomer of the TR-RXR-TRE complex, corepressors get released paving way for the binding of coactivators, thereby inducing the transcription of T 3 -responsive genes. Apart from the canonical nuclear signalling mechanism, membrane-mediated signalling by THs occurs through its interaction with plasma membrane integrin ανβ3. The impact of TH status and TR signalling on a broad range of genes makes studying its effect in vivo a difficult task. Studies on knock-in/out/mutant animal models and humans harboring several mutations of TR isoforms have helped explain various disorders of TH action, particularly the hypothyroid condition associated with the resistance to TH action. The aim of this review is to provide the readers with the information on THs biosynthesis along with the recent progress in TR signalling and its physiological impact on human health.
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人甲状腺激素受体在健康和疾病中的最新进展:化学、生理学和病理生理学
碘甲状腺原氨酸,四碘和三碘甲状腺原氨酸(t4和t3),通常被称为甲状腺激素(THs),由甲状腺分泌。甲状腺激素通过特定的核受体(TRs)影响身体各器官的生长和分化,这些核受体属于核受体超家族。虽然甲状腺分泌的主要是t4(仍与其血清结合蛋白结合),但t3是具有生物活性的TH。游离t4通过特定的转运体进入靶细胞,并通过细胞质5'脱碘酶的细胞特异性异构体转化为t3,该异构体以组织特异性的方式调节循环t3水平及其对核tr的可用性。然后,在nadph依赖的细胞质转运体的帮助下,t3转运到细胞核,在那里它与TR亚型(TRα和TRβ)的单体结合。在与t3结合之前,TR单体与9-顺式维甲酸或类维甲酸X受体(RXR)二聚体结合,TR-RXR异源二聚体与辅抑制因子结合,与靶基因中的特异性TR反应元件(TRE)结合。当t3与TR- rxr - tre复合物的TR单体结合时,协同抑制因子释放,为协同激活因子的结合铺平道路,从而诱导t3应答基因的转录。除了典型的核信号传导机制外,它还通过与质膜整合素ανβ3的相互作用实现膜介导的信号传导。TH状态和TR信号对多种基因的影响使得研究其在体内的作用成为一项艰巨的任务。对敲入/敲出/突变动物模型和携带多种TR异构体突变的人类的研究有助于解释各种TH作用障碍,特别是与TH作用抵抗相关的甲状腺功能减退。本文就三手藤的生物合成、三手藤信号转导的最新进展及其对人体健康的生理影响作一综述。
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