Thyroid Signaling is the cascade initiated by the binding of active thyroid hormones, primarily triiodothyronine (T3), to nuclear receptors within target cells throughout the body, regulating basal metabolic rate and development. This signaling dictates the speed and efficiency of cellular energy processing and protein synthesis across nearly all organ systems. It is a master regulator of systemic metabolic tempo.
Origin
This is a cornerstone concept in classical endocrinology, tracing back to the discovery of the thyroid gland’s critical role in metabolism and growth. The term signifies the entire process from hormone secretion to downstream genomic effects. It is the chemical command for systemic energy utilization.
Mechanism
T4 is converted to the active T3 form, which then translocates to the nucleus to bind to Thyroid Hormone Response Elements (TREs) on DNA, either promoting or repressing gene transcription. This direct genomic action alters the production of metabolic enzymes and structural proteins, thus controlling oxygen consumption and heat production. The integrity of this nuclear binding dictates the overall physiological state.
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