Probing the role of ceramide hydroxylation in skin barrier lipid models by 2H solid-state NMR spectroscopy and X-ray powder diffraction
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
29408487
DOI
10.1016/j.bbamem.2018.02.003
PII: S0005-2736(18)30044-0
Knihovny.cz E-resources
- Keywords
- Hydroxylated skin ceramides, Lipid packing, Model membranes, Order parameter, Thermotropic phase behavior,
- MeSH
- Models, Biological MeSH
- Ceramides chemistry metabolism MeSH
- Cholesterol chemistry MeSH
- Deuterium chemistry MeSH
- Hydroxylation physiology MeSH
- Skin chemistry metabolism MeSH
- Humans MeSH
- Lipid Bilayers chemistry metabolism MeSH
- Magnetic Resonance Spectroscopy methods MeSH
- Cell Membrane Permeability MeSH
- Powder Diffraction methods MeSH
- X-Rays MeSH
- Skin Temperature physiology MeSH
- Temperature MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Ceramides MeSH
- Cholesterol MeSH
- Deuterium MeSH
- Lipid Bilayers MeSH
In this work, we studied model stratum corneum lipid mixtures composed of the hydroxylated skin ceramides N-lignoceroyl 6-hydroxysphingosine (Cer[NH]) and α-hydroxylignoceroyl phytosphingosine (Cer[AP]). Two model skin lipid mixtures of the composition Cer[NH] or Cer[AP], N-lignoceroyl sphingosine (Cer[NS]), lignoceric acid (C24:0) and cholesterol in a 0.5:0.5:1:1 molar ratio were compared. Model membranes were investigated by differential scanning calorimetry and 2H solid-state NMR spectroscopy at temperatures from 25 °C to 80 °C. Each component of the model mixture was specifically deuterated for selective detection by 2H NMR. Thus, the exact phase composition of the mixture at varying temperatures could be quantified. Moreover, using X-ray powder diffraction we investigated the lamellar phase formation. From the solid-state NMR and DSC studies, we found that both hydroxylated Cer[NH] and Cer[AP] exhibit a similar phase behavior. At physiological skin temperature of 32 °C, the lipids form a crystalline (orthorhombic) phase. With increasing temperature, most of the lipids become fluid and form a liquid-crystalline phase, which converts to the isotropic phase at higher temperatures (65-80 °C). Interestingly, lignoceric acid in the Cer[NH]-containing mixture has a tendency to form two types of fluid phases at 65 °C. This tendency was also observed in Cer[AP]-containing membranes at 80 °C. While Cer[AP]-containing lipid models formed a short periodicity phase featuring a repeat spacing of d = 5.4 nm, in the Cer[NH]-based model skin lipid membranes, the formation of unusual long periodicity phase with a repeat spacing of d = 10.7 nm was observed.
References provided by Crossref.org
Polymorphism, Nanostructures, and Barrier Properties of Ceramide-Based Lipid Films
Behavior of 1-Deoxy-, 3-Deoxy- and N-Methyl-Ceramides in Skin Barrier Lipid Models
Long and very long lamellar phases in model stratum corneum lipid membranes