x
Filter:
Filters applied
- Regular Research ArticlesRemove Regular Research Articles filter
- Radner, Franz PWRemove Radner, Franz PW filter
- Journal of Lipid ResearchRemove Journal of Lipid Research filter
Publication Date
Please choose a date range between 2021 and 2022.
Author
- Chalhoub, Gabriel1
- Eisner, Helgit1
- Haemmerle, Guenter1
- Kien, Benedikt1
- Kolleritsch, Stephanie1
- Maresch, Lisa K1
- Meyer, Jason M1
- Oberer, Monika1
- Ondrejčeková, Veronika1
- Opálka, Lukáš1
- Pajed, Laura1
- Rosina, Philipp1
- Schicho, Rudolf1
- Schoiswohl, Gabriele1
- Svatošová, Linda1
- Taschler, Ulrike1
- Tilp, Anna1
- Vávrová, Kateřina1
Regular Research Articles
2 Results
- Research ArticleOpen Access
ω-O-Acylceramides but not ω-hydroxy ceramides are required for healthy lamellar phase architecture of skin barrier lipids
Journal of Lipid ResearchVol. 63Issue 6100226Published online: May 11, 2022- Lukáš Opálka
- Jason M. Meyer
- Veronika Ondrejčeková
- Linda Svatošová
- Franz P.W. Radner
- Kateřina Vávrová
Cited in Scopus: 2Epidermal omega-O-acylceramides (ω-O-acylCers) are essential components of a competent skin barrier. These unusual sphingolipids with ultralong N-acyl chains contain linoleic acid esterified to the terminal hydroxyl of the N-acyl, the formation of which requires the transacylase activity of patatin-like phospholipase domain containing 1 (PNPLA1). In ichthyosis with dysfunctional PNPLA1, ω-O-acylCer levels are significantly decreased, and ω-hydroxylated Cers (ω-OHCers) accumulate. Here, we explore the role of the linoleate moiety in ω-O-acylCers in the assembly of the skin lipid barrier. - Research ArticleOpen Access
Carboxylesterase 2 proteins are efficient diglyceride and monoglyceride lipases possibly implicated in metabolic disease
Journal of Lipid ResearchVol. 62100075Published online: April 16, 2021- Gabriel Chalhoub
- Stephanie Kolleritsch
- Lisa K. Maresch
- Ulrike Taschler
- Laura Pajed
- Anna Tilp
- and others
Cited in Scopus: 0Carboxylesterase 2 (CES2/Ces2) proteins exert established roles in (pro)drug metabolism. Recently, human and murine CES2/Ces2c have been discovered as triglyceride (TG) hydrolases implicated in the development of obesity and fatty liver disease. The murine Ces2 family consists of seven homologous genes as opposed to a single CES2 gene in humans. However, the mechanistic role of Ces2 protein family members is not completely understood. In this study, we examined activities of all Ces2 members toward TGs, diglycerides (DGs), and monoglycerides (MGs) as the substrate.