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박지영

Park, Jiyoung
Molecular Metabolism Lab.
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Activation of invariant natural killer T cells stimulates adipose tissue remodeling via adipocyte death and birth in obesity

Author(s)
Park, JeuHuh, Jin YoungOh, JiyoungKim, Jong InHan, Sang MunShin, Kyung CheulJeon, Yong GeunChoe, Sung SikPark, JiyoungKim, Jae Bum
Issued Date
2019-12
DOI
10.1101/gad.329557.119.
URI
https://scholarworks.unist.ac.kr/handle/201301/30655
Fulltext
http://genesdev.cshlp.org/content/33/23-24/1657
Citation
GENES & DEVELOPMENT, v.33, no.23-24, pp.1657 - 1672
Abstract
In obesity, adipose tissue undergoes dynamic remodeling processes such as adipocyte hypertrophy, hypoxia, immune responses, and adipocyte death. However, whether and how invariant natural killer T (iNKT) cells contribute to adipose tissue remodeling are elusive. In this study, we demonstrate that iNKT cells remove unhealthy adipocytes and stimulate the differentiation of healthy adipocytes. In obese adipose tissue, iNKT cells were abundantly found nearby dead adipocytes. FasL-positive adipose iNKT cells exerted cytotoxic effects to eliminate hypertrophic and pro-inflammatory Fas-positive adipocytes. Furthermore, in vivo adipocyte-lineage tracing mice model showed that activation of iNKT cells by alpha-galactosylceramide promoted adipocyte turnover, eventually leading to potentiation of the insulin-dependent glucose uptake ability in adipose tissue. Collectively, our data propose a novel role of adipose iNKT cells in the regulation of adipocyte turnover in obesity.
Publisher
Cold Spring Harbor Laboratory Press
ISSN
0890-9369
Keyword (Author)
iNKT celladipocyte deathadipocyte turnoveradipogenesisadipose tissue remodeling
Keyword
IN-VIVO IDENTIFICATIONINSULIN-RESISTANCENKT CELLSGLUCOSE-TOLERANCEAPOPTOSISSIZEINFLAMMATIONFASPERFORINMACROPHAGES

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