Abstract

15-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.

Details

Title
Anti-inflammatory role of 15-lipoxygenase contributes to the maintenance of skin integrity in mice
Author
Sang-Nam, Kim 1 ; Akindehin, Seun 1 ; Hyun-Jung, Kwon 1 ; Yeon-Ho Son 1 ; Saha, Abhirup 1 ; Young-Suk, Jung 2 ; Je-Kyung Seong 3 ; Kyung-Min, Lim 4   VIAFID ORCID Logo  ; Jong-Hyuk Sung 1 ; Krishna Rao Maddipati 5 ; Yun-Hee, Lee 1   VIAFID ORCID Logo 

 College of Pharmacy, Yonsei University, Incheon, South Korea 
 College of Pharmacy, Pusan National University, Busan, South Korea 
 College of Veterinary Medicine, Seoul National University, Korea Mouse Phenotyping Center, Seoul, South Korea 
 College of Pharmacy, Ewha Womans University, Seoul, South Korea 
 Lipidomics Core Facility and department of Pathology, Wayne State University, School of Medicine, Detroit, Michigan, USA 
Pages
1-11
Publication year
2018
Publication date
Jun 2018
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2053314295
Copyright
© 2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.