Steroid Signaling describes the complex, multi-step process by which lipophilic steroid hormones, such as cortisol, testosterone, and estrogen, transmit information from the extracellular environment to the cell’s nucleus, ultimately altering gene expression and protein synthesis. This is a fundamental mechanism of endocrinology, governing physiological processes including metabolism, immune function, and sexual differentiation. The integrity of this signaling pathway is paramount for systemic hormonal health.
Origin
This concept is a cornerstone of classical endocrinology, established with the discovery of intracellular steroid receptors and the understanding of how these hormones influence transcription. The term emphasizes the entire cascade, from hormone synthesis and transport to receptor binding and genomic action. It represents the primary mode of action for all cholesterol-derived hormones.
Mechanism
The mechanism is primarily genomic, involving the passive diffusion of the steroid hormone across the cell membrane due to its lipid solubility, followed by binding to a specific intracellular receptor, either in the cytoplasm or the nucleus. The resulting hormone-receptor complex then acts as a transcription factor, binding to specific DNA sequences, known as hormone response elements, to either activate or repress the transcription of target genes. There are also non-genomic, rapid effects mediated by cell surface receptors that modulate ion channels or second messenger systems.
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