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Updated: Jun 12, 2026

Immuno-fluorescent Labeling of Microtubules and Centrosomal Proteins in Ex Vivo Intestinal Tissue and 3D In Vitro Intestinal Organoids
Published on: December 13, 2017
Domains of increased thickness in microvillar membranes of the small intestinal enterocyte
Andreas H Kunding1, Sune M Christensen, E Michael Danielsen
1Bio-Nanotechnology Laboratory, Department of Chemistry & Nano-Science Center, University of Copenhagen, Copenhagen, Denmark.
Abstract:
The apical surface of the enterocyte is sculpted into a dense array of cylindrical microvillar protrusions by supporting actin filaments. Membrane microdomains (rafts) enriched in cholesterol and glycosphingolipids comprise roughly 50% of the microvillar membrane and play a vital role in orchestrating absorptive/digestive action of dietary nutrients at this important cellular interface. Increased membrane thickness is believed to be a morphological characteristic of rafts. Thus, we investigated whether the high contents of lipid rafts in the microvillar membrane is reflected in local variations in membrane thickness. We measured membrane thickness directly from electron micrographs of sections of fixed mucosal tissue. Indeed, mapping of the microvillar membrane revealed a biphasic distribution of membrane thickness. As a point of reference the thickness distribution of the basolateral membrane was clearly monophasic. The encountered domains of increased thickness (DITs) occupied 48% of the microvillar membrane and from the data we estimated the area of a single DIT to have a lower limit of 600 nm(2). In other experiments we mapped the organization of biochemically defined lipid rafts by immunogold labeling of alkaline phosphatase, a well documented raft marker. Strikingly, the alkaline phosphatase localized to distinct regions of the membrane in a pattern similar to the observed distribution of DITs. Although we were unable to measure membrane thickness directly on the immunogold labeled specimens, and thereby establish an unequivocal connection between DITs and rafts, we conclude that the brush border membrane of the enterocyte contains microdomains distinguishable both by membrane morphology and protein composition.
Insights
Enterocyte microvillar membranes contain distinct domains of increased thickness, correlating with lipid raft distribution. These specialized membrane structures are crucial for nutrient absorption and digestion.
Area of Science:
- Cell Biology
- Membrane Biology
- Gastroenterology
Background:
- Enterocytes feature microvilli on their apical surface, essential for nutrient absorption.
- Microvilli membranes are rich in lipid rafts, cholesterol- and glycosphingolipid-enriched domains vital for digestive functions.
- Increased membrane thickness is a proposed characteristic of lipid rafts.
Purpose of the Study:
- To investigate if high lipid raft content in enterocyte microvilli correlates with local variations in membrane thickness.
- To characterize the morphology and protein composition of microvillar membrane domains.
Main Methods:
- Direct measurement of membrane thickness from electron micrographs of fixed enterocyte mucosal tissue.
- Mapping of membrane thickness distribution across microvillar and basolateral membranes.
- Immunogold labeling using alkaline phosphatase as a lipid raft marker to map raft organization.
Main Results:
- Microvillar membrane thickness exhibited a biphasic distribution, unlike the monophasic distribution of the basolateral membrane.
- Domains of increased thickness (DITs) constituted 48% of the microvillar membrane surface area.
- Alkaline phosphatase, a raft marker, localized to distinct membrane regions mirroring the distribution of DITs.
Conclusions:
- The enterocyte brush border membrane possesses microdomains characterized by distinct membrane thickness and protein composition.
- These findings suggest a strong correlation between membrane morphology (thickness) and lipid raft organization in microvilli.
- The study provides morphological and compositional evidence for specialized microdomains within the enterocyte microvillar membrane.
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