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Published on: October 18, 2013
A model membrane approach to the epidermal permeability barrier: an X-ray diffraction study
J A Bouwstra1, J Thewalt, G S Gooris
1Leiden/Amsterdam Center for Drug Research, Gorlaeus Laboratories, Leiden University, The Netherlands.
Insights
Mammalian skin barrier function relies on lamellar lipid structures. Ceramides, even with cholesterol, form crystalline phases crucial for skin permeability, unlike sphingomyelin which forms fluid phases.
Area of Science:
- Biophysics
- Dermatology
- Materials Science
Background:
- Mammalian skin permeability is primarily regulated by lipid lamellar structures in the stratum corneum.
- These lamellae differ from typical biological membranes due to a unique lipid composition: ceramides, cholesterol, and free fatty acids.
Purpose of the Study:
- To investigate the phase behavior of ceramide-cholesterol lipid dispersions.
- To compare the structural properties of ceramide-based lamellae with sphingomyelin-based lamellae.
Main Methods:
- Deuterium Nuclear Magnetic Resonance (NMR) spectroscopy was used to study lipid dispersions.
- X-ray diffraction was employed to analyze the structural phases of the dispersions at pH 5.2.
Main Results:
- Ceramide and cholesterol dispersions exhibited complex crystalline phases between room temperature and approximately 40°C.
- The majority of crystalline cholesterol was integrated within the ceramide phase, not separate.
- Analogous dispersions with sphingomyelin showed a fluid lamellar phase under identical conditions.
Conclusions:
- Ceramides, even with significant cholesterol, can form crystalline lamellar structures.
- These ceramide-cholesterol crystalline structures may play a vital role in the epidermal permeability barrier.
- Interactions between ceramides and cholesterol in other biological membranes could lead to unique physical properties.
Abstract:
The permeability of mammalian skin is determined in large part by lamellar lipid domains packed between cells of the upper layer of the epidermis, the stratum comeum. Although these lamellae have features in common with typical biological membranes, they differ in having a lipid population composed mainly of ceramides, cholesterol, and free fatty acids. In our initial studies of the relationship between lipid composition and phase behavior in this unusual system, we used deuterium NMR [Kitson et al. (1994) Biochemistry 33, 6707-6715] to examine aqueous dispersions of nonhydroxylated bovine brain ceramide, cholesterol, and perdeuterated palmitic acid, and found complex phase behavior as a function of temperature and pH, whereas analogous dispersions in which sphingomyelin replaced ceramide resulted in spectra consistent with a fluid lamellar phase under the same conditions. To extend these observations, we examined the same dispersions at pH 5.2 by means of X-ray diffraction. The significant findings are as follows: (1) the ceramide dispersions form complex crystalline phases between room temperature and about 40 degrees C; (2) the majority of the crystalline cholesterol is not in a separate phase; and (3) the analogous sphingomyelin dispersions form a fluid lamellar phase under the same conditions. We conclude that ceramides, even in the presence of considerable mole fractions of cholesterol, can form crystalline lamellar structures. We suggest that the existence of such structures in stratum corneum may be important in the function of the epidermal permeability barrier, and that the interaction between ceramide and cholesterol in other biological membranes may result in regions having unique physical properties.
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