Cargando…

The dual lipid desaturase/hydroxylase DEGS2 controls phytoceramide levels necessary to counter intestinal inflammation

Intestinal immunity is dependent on barrier function to maintain quiescence. The mechanisms for the maintenance of this barrier are not fully understood. Delta 4-desaturase, sphingolipid 2 (DEGS2) is a lipid desaturase and hydroxylase that catalyzes the synthesis of ceramide and phytoceramide from d...

Descripción completa

Detalles Bibliográficos
Autores principales: Song, Ran, Fond, Aaron, Li, Xiaohong, Tang, Miao, Zhan, Xiaoming, Gordillo, Ruth, Moresco, Eva Marie Y., Beutler, Bruce, Turer, Emre E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499023/
https://www.ncbi.nlm.nih.gov/pubmed/37589563
http://dx.doi.org/10.1242/dmm.050043
_version_ 1785105636182196224
author Song, Ran
Fond, Aaron
Li, Xiaohong
Tang, Miao
Zhan, Xiaoming
Gordillo, Ruth
Moresco, Eva Marie Y.
Beutler, Bruce
Turer, Emre E.
author_facet Song, Ran
Fond, Aaron
Li, Xiaohong
Tang, Miao
Zhan, Xiaoming
Gordillo, Ruth
Moresco, Eva Marie Y.
Beutler, Bruce
Turer, Emre E.
author_sort Song, Ran
collection PubMed
description Intestinal immunity is dependent on barrier function to maintain quiescence. The mechanisms for the maintenance of this barrier are not fully understood. Delta 4-desaturase, sphingolipid 2 (DEGS2) is a lipid desaturase and hydroxylase that catalyzes the synthesis of ceramide and phytoceramide from dihydroceramide. Using a forward genetic approach, we found and validated a mutation in Degs2 as causative of increasing susceptibility to colitis and altering the phytoceramide balance in the colon. DEGS2 is expressed in the intestinal epithelium, and the colitis phenotype is dependent on the non-hematopoietic compartment of the mouse. In the absence of DEGS2, the colon lacks phytoceramides and accumulates large amounts of the precursor lipid dihydroceramide. In response to dextran sodium sulfate (DSS)-induced colitis, colonic epithelial cells in DEGS2-deficient mice had increased cell death and decreased proliferation compared to those in wild-type mice. These findings demonstrate that DEGS2 is needed to maintain epithelial integrity, protect against DSS-induced colitis and maintain lipid balance in vivo.
format Online
Article
Text
id pubmed-10499023
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher The Company of Biologists Ltd
record_format MEDLINE/PubMed
spelling pubmed-104990232023-09-14 The dual lipid desaturase/hydroxylase DEGS2 controls phytoceramide levels necessary to counter intestinal inflammation Song, Ran Fond, Aaron Li, Xiaohong Tang, Miao Zhan, Xiaoming Gordillo, Ruth Moresco, Eva Marie Y. Beutler, Bruce Turer, Emre E. Dis Model Mech Research Article Intestinal immunity is dependent on barrier function to maintain quiescence. The mechanisms for the maintenance of this barrier are not fully understood. Delta 4-desaturase, sphingolipid 2 (DEGS2) is a lipid desaturase and hydroxylase that catalyzes the synthesis of ceramide and phytoceramide from dihydroceramide. Using a forward genetic approach, we found and validated a mutation in Degs2 as causative of increasing susceptibility to colitis and altering the phytoceramide balance in the colon. DEGS2 is expressed in the intestinal epithelium, and the colitis phenotype is dependent on the non-hematopoietic compartment of the mouse. In the absence of DEGS2, the colon lacks phytoceramides and accumulates large amounts of the precursor lipid dihydroceramide. In response to dextran sodium sulfate (DSS)-induced colitis, colonic epithelial cells in DEGS2-deficient mice had increased cell death and decreased proliferation compared to those in wild-type mice. These findings demonstrate that DEGS2 is needed to maintain epithelial integrity, protect against DSS-induced colitis and maintain lipid balance in vivo. The Company of Biologists Ltd 2023-09-08 /pmc/articles/PMC10499023/ /pubmed/37589563 http://dx.doi.org/10.1242/dmm.050043 Text en © 2023. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Song, Ran
Fond, Aaron
Li, Xiaohong
Tang, Miao
Zhan, Xiaoming
Gordillo, Ruth
Moresco, Eva Marie Y.
Beutler, Bruce
Turer, Emre E.
The dual lipid desaturase/hydroxylase DEGS2 controls phytoceramide levels necessary to counter intestinal inflammation
title The dual lipid desaturase/hydroxylase DEGS2 controls phytoceramide levels necessary to counter intestinal inflammation
title_full The dual lipid desaturase/hydroxylase DEGS2 controls phytoceramide levels necessary to counter intestinal inflammation
title_fullStr The dual lipid desaturase/hydroxylase DEGS2 controls phytoceramide levels necessary to counter intestinal inflammation
title_full_unstemmed The dual lipid desaturase/hydroxylase DEGS2 controls phytoceramide levels necessary to counter intestinal inflammation
title_short The dual lipid desaturase/hydroxylase DEGS2 controls phytoceramide levels necessary to counter intestinal inflammation
title_sort dual lipid desaturase/hydroxylase degs2 controls phytoceramide levels necessary to counter intestinal inflammation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499023/
https://www.ncbi.nlm.nih.gov/pubmed/37589563
http://dx.doi.org/10.1242/dmm.050043
work_keys_str_mv AT songran theduallipiddesaturasehydroxylasedegs2controlsphytoceramidelevelsnecessarytocounterintestinalinflammation
AT fondaaron theduallipiddesaturasehydroxylasedegs2controlsphytoceramidelevelsnecessarytocounterintestinalinflammation
AT lixiaohong theduallipiddesaturasehydroxylasedegs2controlsphytoceramidelevelsnecessarytocounterintestinalinflammation
AT tangmiao theduallipiddesaturasehydroxylasedegs2controlsphytoceramidelevelsnecessarytocounterintestinalinflammation
AT zhanxiaoming theduallipiddesaturasehydroxylasedegs2controlsphytoceramidelevelsnecessarytocounterintestinalinflammation
AT gordilloruth theduallipiddesaturasehydroxylasedegs2controlsphytoceramidelevelsnecessarytocounterintestinalinflammation
AT morescoevamariey theduallipiddesaturasehydroxylasedegs2controlsphytoceramidelevelsnecessarytocounterintestinalinflammation
AT beutlerbruce theduallipiddesaturasehydroxylasedegs2controlsphytoceramidelevelsnecessarytocounterintestinalinflammation
AT tureremree theduallipiddesaturasehydroxylasedegs2controlsphytoceramidelevelsnecessarytocounterintestinalinflammation
AT songran duallipiddesaturasehydroxylasedegs2controlsphytoceramidelevelsnecessarytocounterintestinalinflammation
AT fondaaron duallipiddesaturasehydroxylasedegs2controlsphytoceramidelevelsnecessarytocounterintestinalinflammation
AT lixiaohong duallipiddesaturasehydroxylasedegs2controlsphytoceramidelevelsnecessarytocounterintestinalinflammation
AT tangmiao duallipiddesaturasehydroxylasedegs2controlsphytoceramidelevelsnecessarytocounterintestinalinflammation
AT zhanxiaoming duallipiddesaturasehydroxylasedegs2controlsphytoceramidelevelsnecessarytocounterintestinalinflammation
AT gordilloruth duallipiddesaturasehydroxylasedegs2controlsphytoceramidelevelsnecessarytocounterintestinalinflammation
AT morescoevamariey duallipiddesaturasehydroxylasedegs2controlsphytoceramidelevelsnecessarytocounterintestinalinflammation
AT beutlerbruce duallipiddesaturasehydroxylasedegs2controlsphytoceramidelevelsnecessarytocounterintestinalinflammation
AT tureremree duallipiddesaturasehydroxylasedegs2controlsphytoceramidelevelsnecessarytocounterintestinalinflammation