Skip to main content
Article

Membrane lipidome of an epithelial cell line

Júlio L. SampaioMax Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany;Mathias J. GerlMax Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany;Christian KloseMax Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany;Christer S. EjsingDepartment of Biochemistry and Molecular Biology, University of Southern Denmark, 55 Campusvej, DK-5230 Odense, Denmark; andHartmut BeugResearch Institute of Molecular Pathology, 1030 Vienna, AustriaKai SimonsMax Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany;Andrej ShevchenkoMax Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany;
2011en
ABI

Abstract

Tissue differentiation is an important process that involves major cellular membrane remodeling. We used Madin-Darby canine kidney cells as a model for epithelium formation and investigated the remodeling of the total cell membrane lipidome during the transition from a nonpolarized morphology to an epithelial morphology and vice versa. To achieve this, we developed a shotgun-based lipidomics workflow that enabled the absolute quantification of mammalian membrane lipidomes with minimal sample processing from low sample amounts. Epithelial morphogenesis was accompanied by a major shift from sphingomyelin to glycosphingolipid, together with an increase in plasmalogen, phosphatidylethanolamine, and cholesterol content, whereas the opposite changes took place during an epithelial-to-mesenchymal transition. Moreover, during polarization, the sphingolipids became longer, more saturated, and more hydroxylated as required to generate an apical membrane domain that serves as a protective barrier for the epithelial sheet.

Identifiers

Citations and references

Cited by 20 references