Ablation of ceramide synthase 2 exacerbates dextran sodium sulphate-induced colitis in mice due to increased intestinal permeability
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kim, Ye-Ryung | - |
dc.contributor.author | Volpert, Giora | - |
dc.contributor.author | Shin, Kyong-Oh | - |
dc.contributor.author | Kim, So-Yeon | - |
dc.contributor.author | Shin, Sun-Hye | - |
dc.contributor.author | Lee, Younghay | - |
dc.contributor.author | Sung, Sun Hee | - |
dc.contributor.author | Lee, Yong-Moon | - |
dc.contributor.author | Ahn, Jung-Hyuck | - |
dc.contributor.author | Pewzner-Jung, Yael | - |
dc.contributor.author | Park, Woo-Jae | - |
dc.contributor.author | Futerman, Anthony H. | - |
dc.contributor.author | Park, Joo-Won | - |
dc.date.accessioned | 2024-01-08T22:37:09Z | - |
dc.date.available | 2024-01-08T22:37:09Z | - |
dc.date.issued | 2017-12 | - |
dc.identifier.issn | 1582-1838 | - |
dc.identifier.issn | 1582-4934 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/69629 | - |
dc.description.abstract | Ceramides mediate crucial cellular processes including cell death and inflammation and have recently been implicated in inflammatory bowel disease. Ceramides consist of a sphingoid long-chain base to which fatty acids of various length can be attached. We now investigate the effect of alerting the ceramide acyl chain length on a mouse model of colitis. Ceramide synthase (CerS) 2 null mice, which lack very-long acyl chain ceramides with concomitant increase of long chain bases and C16-ceramides, were more susceptible to dextran sodium sulphate-induced colitis, and their survival rate was markedly decreased compared with that of wild-type littermates. Using mixed bone-marrow chimeric mice, we showed that the host environment is primarily responsible for intestinal barrier dysfunction and increased intestinal permeability. In the colon of CerS2 null mice, the expression of junctional adhesion molecule-A was markedly decreased and the phosphorylation of myosin light chain 2 was increased. In vitro experiments using Caco-2 cells also confirmed an important role of CerS2 in maintaining epithelial barrier function; CerS2-knockdown via CRISPR-Cas9 technology impaired barrier function. In vivo myriocin administration, which normalized long-chain bases and C16-ceramides of the colon of CerS2 null mice, increased intestinal permeability as measured by serum FITC-dextran levels, indicating that altered SLs including deficiency of very-long-chain ceramides are critical for epithelial barrier function. In conclusion, deficiency of CerS2 influences intestinal barrier function and the severity of experimental colitis and may represent a potential mechanism for inflammatory bowel disease pathogenesis. | - |
dc.format.extent | 14 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | WILEY | - |
dc.title | Ablation of ceramide synthase 2 exacerbates dextran sodium sulphate-induced colitis in mice due to increased intestinal permeability | - |
dc.type | Article | - |
dc.identifier.doi | 10.1111/jcmm.13267 | - |
dc.identifier.bibliographicCitation | JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, v.21, no.12, pp 3565 - 3578 | - |
dc.description.isOpenAccess | Y | - |
dc.identifier.wosid | 000418574500038 | - |
dc.identifier.scopusid | 2-s2.0-85023198203 | - |
dc.citation.endPage | 3578 | - |
dc.citation.number | 12 | - |
dc.citation.startPage | 3565 | - |
dc.citation.title | JOURNAL OF CELLULAR AND MOLECULAR MEDICINE | - |
dc.citation.volume | 21 | - |
dc.type.docType | Article | - |
dc.publisher.location | 미국 | - |
dc.subject.keywordAuthor | inflammatory bowel disease | - |
dc.subject.keywordAuthor | ceramide | - |
dc.subject.keywordAuthor | sphingolipid | - |
dc.subject.keywordAuthor | acyl chains | - |
dc.subject.keywordAuthor | dextran sodium sulphate | - |
dc.subject.keywordPlus | EPITHELIAL BARRIER FUNCTION | - |
dc.subject.keywordPlus | INFLAMMATORY-BOWEL-DISEASE | - |
dc.subject.keywordPlus | ACYL-CHAIN LENGTH | - |
dc.subject.keywordPlus | TIGHT-JUNCTION | - |
dc.subject.keywordPlus | SPHINGOLIPID METABOLISM | - |
dc.subject.keywordPlus | INSULIN-RESISTANCE | - |
dc.subject.keywordPlus | MEMBRANE-FLUIDITY | - |
dc.subject.keywordPlus | FUMONISIN B-1 | - |
dc.subject.keywordPlus | CELLS | - |
dc.subject.keywordPlus | LIVER | - |
dc.relation.journalResearchArea | Cell Biology | - |
dc.relation.journalResearchArea | Research & Experimental Medicine | - |
dc.relation.journalWebOfScienceCategory | Cell Biology | - |
dc.relation.journalWebOfScienceCategory | Medicine, Research & Experimental | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
84, Heukseok-ro, Dongjak-gu, Seoul, Republic of Korea (06974)02-820-6194
COPYRIGHT 2019 Chung-Ang University All Rights Reserved.
Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.