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Anti-inflammatory role of 15-lipoxygenase contributes to the maintenance of skin integrity in mice

DC Field Value Language
dc.contributor.authorKim, Sang-Nam-
dc.contributor.authorAkindehin, Seun-
dc.contributor.authorKwon, Hyun-Jung-
dc.contributor.authorSon, Yeon-Ho-
dc.contributor.authorSaha, Abhirup-
dc.contributor.authorJung, Young-Suk-
dc.contributor.authorSeong, Je-Kyung-
dc.contributor.authorLim, Kyung-Min-
dc.contributor.authorSung, Jong-Hyuk-
dc.contributor.authorMaddipati, Krishna Rao-
dc.contributor.authorLee, Yun-Hee-
dc.date.accessioned2024-08-08T01:31:39Z-
dc.date.available2024-08-08T01:31:39Z-
dc.date.created2019-07-09-
dc.date.created2019-07-09-
dc.date.issued2018-06-
dc.identifier.citationScientific Reports, Vol.8 No.1, p. 8856-
dc.identifier.issn2045-2322-
dc.identifier.urihttps://hdl.handle.net/10371/206479-
dc.description.abstract15-lipoxygenase is involved in the generation of specialized pro-resolving lipid mediators that play essential roles in resolution and inflammatory responses. Here, we investigated anti-inflammatory role of Alox15 in skin homeostasis. We demonstrated that knockout (KO) of Alox15 led to hair loss and disrupted the structural integrity of the dorsal skin. Alox15 KO resulted in loss of hair follicle stem cells and abnormal transition of dermal adipocytes into fibroblasts. Alox15 deficiency increased infiltration of proinflammatory macrophages and upregulated proinflammatory and necroptotic signaling in dermal adipose tissue in the dorsal skin. Lipidomic analysis revealed severe loss of resolvin D2 in the dorsal skin of Alox15 KO mice compared to wild type controls. Treatment with resolvin D2 reduced skin inflammation in Alox15 KO mice. Collectively, these results indicate that Alox15-mediated production of resolvin D2 is required to maintain skin integrity by suppressing dermal inflammation.-
dc.language영어-
dc.publisherNature Publishing Group-
dc.titleAnti-inflammatory role of 15-lipoxygenase contributes to the maintenance of skin integrity in mice-
dc.typeArticle-
dc.identifier.doi10.1038/s41598-018-27221-7-
dc.citation.journaltitleScientific Reports-
dc.identifier.wosid000434777700002-
dc.identifier.scopusid2-s2.0-85048346643-
dc.citation.number1-
dc.citation.startpage8856-
dc.citation.volume8-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorSeong, Je-Kyung-
dc.contributor.affiliatedAuthorLee, Yun-Hee-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusLIPID MEDIATORS-
dc.subject.keywordPlusRESOLVIN D2-
dc.subject.keywordPlusMYOFIBROBLASTS-
dc.subject.keywordPlusINFLAMMATION-
dc.subject.keywordPlusNECROPTOSIS-
dc.subject.keywordPlusMACROPHAGES-
dc.subject.keywordPlusADIPOCYTES-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusMODEL-
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  • College of Veterinary Medicine
  • Department of Veterinary Medicine
Research Area Metabolic syndrome model construction and omics research, Mouse locomotion and metabolic phenotyping analysis, Study of immune regulatory response in obesity, 대사증후군 모델 구축 및 오믹스 연구, 마우스 운동 및 대사 표현형 분석, 비만에서의 면역 조절 반응 연구

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