Instituto de Investigaciones Biomédicas "Sols-Morreale", Consejo Superior de Investigaciones Científicas and Universidad Autónoma de Madrid, Madrid, Spain.
Methods Mol Biol. 2025;2876:17-34. doi: 10.1007/978-1-0716-4252-8_2.
The thyroid hormones, thyroxine (T4) and triiodothyronine (T3), are pivotal in regulating various physiological processes including growth, development, and metabolism. The biological actions of thyroid hormones are primarily initiated by binding to nuclear thyroid hormone receptors (TRs). These receptors, belonging to the superfamily of nuclear receptors, act as ligand-dependent transcription factors. Transcriptional regulation by TRs is mediated by the recruitment of coregulators, governing activation and repression of target genes, thereby modulating cellular responses to thyroid hormones. Beyond this canonical genomic pathway, TH can regulate the expression of genes not directly bound by TRs through cross-talk mechanisms with other transcription factors and signaling pathways. Thyroid hormones can also elicit rapid non-genomic effects, potentially mediated by extranuclear TR proteins or by interactions with membrane receptors such as integrin αvβ3. This non-genomic mode of action adds another layer of complexity to the diverse array of physiological responses orchestrated by thyroid hormones, expanding our understanding of their multifaceted actions.
甲状腺激素,包括甲状腺素(T4)和三碘甲状腺原氨酸(T3),在调节各种生理过程中起着关键作用,包括生长、发育和代谢。甲状腺激素的生物学作用主要是通过与核甲状腺激素受体(TRs)结合而启动的。这些受体属于核受体超家族,作为配体依赖性转录因子发挥作用。TR 介导的转录调节是通过募集共调节剂来实现的,共调节剂可以调节靶基因的激活和抑制,从而调节细胞对甲状腺激素的反应。除了这种经典的基因组途径外,TH 还可以通过与其他转录因子和信号通路的交叉对话机制,调节不直接与 TR 结合的基因的表达。甲状腺激素还可以通过核外 TR 蛋白或与整合素 αvβ3 等膜受体的相互作用,产生快速的非基因组效应。这种非基因组作用模式为甲状腺激素协调的多种生理反应增加了另一层复杂性,扩展了我们对其多方面作用的理解。