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Clinically confirmed DEL-1 as a myokine attenuates lipid-induced inflammation and insulin resistance in 3T3-L1 adipocytes via AMPK/HO-1- pathway

Authors
Kwon, Chang HyukSun, Jaw LongKim, Myeong JunAbd El-Aty, A. M.Jeong, Ji HoonJung, Tae Woo
Issue Date
Jan-2020
Publisher
TAYLOR & FRANCIS INC
Keywords
Myokine; DEL-1; insulin resistance; inflammation; AMPK; HO-1
Citation
ADIPOCYTE, v.9, no.1, pp 576 - 586
Pages
11
Journal Title
ADIPOCYTE
Volume
9
Number
1
Start Page
576
End Page
586
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/63257
DOI
10.1080/21623945.2020.1823140
ISSN
2162-3945
2162-397X
Abstract
Regular exercise is the first line of therapy for treating obesity-mediated metabolic disorders, including insulin resistance. It has been reported that developmental endothelial locus-1 (DEL-1) enhances macrophage efferocytosis, resulting in inflammation clearance as well as improves insulin resistance in skeletal muscle. However, the relationship between exercise and DEL-1, and the effects of DEL-1 on insulin signalling in adipocytes have not been fully elucidated to date. Protein expression levels were determined by Western blot analysis. Cells were transfected with small interfering (si) RNA to suppress gene expression. Lipid accumulation levels were detected using Oil red-O staining. Proinflammatory cytokine secretion levels were measured using ELISA. DEL-1 expression levels were induced in the skeletal muscle of people who exercised using microarray analysis. Recombinant DEL-1 augmented AMP-activated protein kinase (AMPK) phosphorylation and haem oxygenase (HO)-1 expression to alleviating inflammation and impairment of insulin signalling in 3T3-L1 adipocytes treated with palmitate. siRNA of AMPK or HO-1 also mitigated the effects of DEL-1 on inflammation and insulin resistance. DEL-1 ameliorates inflammation and insulin resistance in differentiated 3T3-L1 cells via AMPK/HO-1 signalling, suggesting that DEL-1 may be the exercise-mediated therapeutic target for treating insulin resistance and type 2 diabetes. [GRAPHICS] .
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