Cellular Receptor Availability describes the absolute number or density of specific membrane or intracellular binding sites present on a target cell that are capable of binding a circulating hormone or ligand. This metric directly dictates the cell’s potential responsiveness to endocrine signals. Low availability implies a degree of functional resistance.
Origin
This concept stems from fundamental receptor pharmacology, defining the physical machinery through which hormones exert their primary action. Understanding availability is crucial because circulating hormone concentration alone does not dictate effect. It establishes the upper limit of cellular response capacity.
Mechanism
Availability is dynamically regulated through processes like ligand-induced internalization and subsequent degradation, or conversely, through upregulation in response to chronic low ligand exposure. Furthermore, the physical state of the cell membrane and the presence of competing molecules can modulate how many receptors are functionally accessible at any given time.
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