Institute of Clinical Physiology, National Research Council of Italy (CNR), Pisa, Italy.
Fondazione CNR-Regione Toscana Gabriele Monasterio, Pisa, Italy.
Endocrinol Metab (Seoul). 2021 Oct;36(5):952-964. doi: 10.3803/EnM.2021.1198. Epub 2021 Oct 21.
Thyroid hormone (TH) signaling is strictly regulated by iodothyronine deiodinase activity, which both preserves the circulating levels of the biologically active triiodothyronine (T3) and regulates TH homeostasis at the local level, in a cell- and time-dependent manner. Three deiodinases have been identified-namely iodothyronine deiodinase 1 (DIO1), DIO2, and DIO3-that differ in their catalytic properties and tissue distribution. The deiodinases represent a dynamic system that changes in the different stages of life according to their functions and roles in various cell types and tissues. Deiodinase activity at the tissue level permits cell-targeted fine regulation of TH homeostasis, mediating the activation (DIO1 and DIO2) and inactivation (DIO3) of THs. Deiodinase homeostasis is the driving force that leads T3-target cells towards customized TH signaling, which takes into account both the hormonal circulating levels and the tissue-specific response. This review analyzes the complex role of deiodinases in physiological and pathological contexts, exploring new challenges and opportunities deriving from a deeper knowledge of the dynamics underlying their roles and functions.
甲状腺激素 (TH) 信号受到碘甲状腺原氨酸脱碘酶活性的严格调节,这种酶以细胞和时间依赖的方式,既能维持循环中生物活性三碘甲状腺原氨酸 (T3) 的水平,又能调节局部 TH 稳态。已经鉴定出三种脱碘酶,即甲状腺素脱碘酶 1 (DIO1)、DIO2 和 DIO3,它们在催化特性和组织分布上有所不同。脱碘酶代表了一个动态系统,根据其在不同细胞类型和组织中的功能和作用,在生命的不同阶段发生变化。组织水平的脱碘酶活性允许针对 TH 稳态进行细胞靶向的精细调节,介导 TH 的激活 (DIO1 和 DIO2) 和失活 (DIO3)。脱碘酶稳态是一种驱动力,使 T3 靶细胞朝着定制化的 TH 信号转导发展,这既考虑了激素的循环水平,又考虑了组织特异性反应。本综述分析了脱碘酶在生理和病理情况下的复杂作用,探讨了从更深层次了解其作用和功能背后的动力学中获得的新挑战和机遇。