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The brush border membrane is a specialized cell membrane in the small intestine and kidney tubules, densely covered with tiny projections called microvilli that greatly increase the absorptive surface area.
The brush border membrane is a specialized cell membrane in the small intestine and kidney tubules, densely covered with tiny projections called microvilli that greatly increase the absorptive surface area.
The brush border membrane is the apical (luminal) surface of epithelial cells that is densely packed with tiny finger-like projections known as microvilli. Under a microscope, these projections resemble the bristles of a brush – hence the name. The brush border membrane is found predominantly in the small intestine (jejunum and ileum) and the proximal renal tubules, though it also occurs in other epithelial tissues such as the gallbladder.
Each individual microvillus is approximately 1–3 micrometers in length and is supported internally by a core of actin filaments. Together, the microvilli of a single intestinal cell (enterocyte) increase the apical surface area by 20- to 40-fold. Combined with the intestinal folds (plicae circulares) and villi, the total absorptive surface area in a healthy adult can reach up to 200 square meters.
The brush border membrane contains a wide variety of transport proteins and channel proteins that facilitate the uptake of nutrients, ions, and water into the cell. Key transporters include the sodium-glucose cotransporter (SGLT1), amino acid transporters, and carriers for fatty acids and vitamins.
Several important digestive enzymes are embedded directly in the brush border membrane, including:
Together with the glycocalyx – a protective carbohydrate layer coating the cell surface – the brush border membrane acts as a selective barrier, preventing pathogens and harmful substances from penetrating the intestinal wall.
Damage to the brush border membrane can have significant health consequences. Conditions associated with brush border dysfunction include:
The brush border membrane is also of major pharmacological relevance. Many orally administered drugs are taken up via transport proteins located in this membrane. Interactions at these transporters can significantly affect the bioavailability of medications. A well-known example involves SGLT2 inhibitors, which target related transport mechanisms in the kidney and are used to treat type 2 diabetes.
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