Small, dynamic, cholesterol- and sphingolipid-rich microdomains within the plasma membrane of a cell. These specialized regions serve as organizational platforms, concentrating specific proteins, receptors, and signaling molecules necessary for efficient cellular communication. Lipid rafts are crucial for the non-genomic actions of steroid hormones and peptide growth factors, acting as cellular signaling hubs.
Origin
The concept of a non-uniform, compartmentalized cell membrane structure emerged in the 1970s, but the term ‘lipid raft’ was formalized in the 1990s following advancements in membrane biophysics. The term reflects the unique lipid composition that causes these regions to ‘float’ as more ordered, thicker domains within the fluid bilayer. Their existence challenges the simplistic fluid mosaic model of the cell membrane.
Mechanism
The high concentration of cholesterol and saturated lipids in the raft structure creates an environment that facilitates the clustering and activation of specific signaling cascades. Certain hormone receptors, including G-protein coupled receptors and some steroid hormone receptors, preferentially localize to these domains upon ligand binding. This spatial organization ensures rapid and localized signal transduction, allowing for efficient integration of extracellular hormonal cues into intracellular responses.
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