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Whole picture of human stratum corneum ceramides, including the chain-length diversity of long-chain bases
| Title: | Whole picture of human stratum corneum ceramides, including the chain-length diversity of long-chain bases |
| Authors: | Suzuki, Madoka Browse this author | | Ohno, Yusuke Browse this author →KAKEN DB | | Kihara, Akio Browse this author →KAKEN DB |
| Keywords: | ceramide | | epidermis | | lipidomics | | long-chain base | | mass spectrometry | | skin barrier | | sphingolipid | | stratum corneum |
| Issue Date: | Jul-2022 |
| Publisher: | Elsevier |
| Journal Title: | Journal of Lipid Research (JLR) |
| Volume: | 63 |
| Issue: | 7 |
| Start Page: | 100235 |
| Publisher DOI: | 10.1016/j.jlr.2022.100235 |
| Abstract: | Ceramides are essential lipids for skin permeability barrier function, and a wide variety of ceramide species exist in the stratum corneum (SC). Although ceramides with long-chain bases (LCBs) of various lengths have been identified in the human SC, a quantitative analysis that distinguishes ceramide species with different LCB chain lengths has not been yet published. Therefore, the whole picture of human SC ceramides remains unclear. Here, we conducted LC/MS/MS analyses to detect individual ceramide species differing in both the LCB and FA chain lengths and quantified 1,327 unbound ceramides and 254 protein-bound ceramides: the largest number of ceramide species reported to date. Ceramides containing an LCB whose chain length was C16-26 were present in the human SC. Of these, C18 (28.6%) was the most abundant, followed by C20 (24.8%) and C22 (12.8%). Each ceramide class had a characteristic distribution of LCB chain lengths and was divided into five groups according to this distribution. There was almost no difference in FA composition between the ceramide species containing LCBs of different chain lengths. Furthermore, we demonstrated that one of the serine palmitoyltransferase (SPT) complexes, SPTLC1/SPTLC3/SPTSSB, was able to produce C16-24 LCBs. The expression levels of all subunits constituting the SPT complexes increased during keratinocyte differentiation, resulting in the observed chain-length diversity of LCBs in the human SC. This study provides a molecular basis for elucidating human SC ceramide diversity and the pathogenesis of skin disorders. |
| Type: | article |
| URI: | http://hdl.handle.net/2115/87014 |
| Appears in Collections: | 薬学研究院 (Faculty of Pharmaceutical Sciences) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)
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