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High Fat Diet Triggers a Reduction in Body Fat Mass in Female Mice Deficient for Utx demethylase.
- Source :
-
Scientific reports [Sci Rep] 2019 Jul 11; Vol. 9 (1), pp. 10036. Date of Electronic Publication: 2019 Jul 11. - Publication Year :
- 2019
-
Abstract
- Obesity increases the risk of metabolic disorders like diabetes mellitus and dyslipidemia. However, how metabolic status is sensed and regulates cellular behavior is unclear. Utx is an H3K27 demethylase that influences adipocyte function in vitro. To examine its role in vivo, we generated mice lacking Utx in adipocytes (UtxAKO). Although all UtxAKO mice grew normally on a normal chow diet (NCD), female UtxAKO mice on a high fat diet (HFD) showed striking reductions in body fat compared to control mice (Ctrl). Gene expression profiling of adipose tissues of HFD-fed UtxAKO female mice revealed decreased expression of rate-limiting enzymes of triacylglycerol synthesis but increased expression of those of cholesterol/steroid hormone synthesis. Moreover, these animals resisted adiposity induced by ovariectomy and exhibited increased estrogen in visceral adipose tissues. Thus, upon HFD feeding, Utx regulates lipid metabolism in adipose tissues by influencing the local hormonal microenvironment. Conversely, Utx deficiency skews lipid catabolism to enhance cholesterol/steroid hormone production and repress obesity.
- Subjects :
- Adipocytes metabolism
Adipose Tissue metabolism
Adiposity physiology
Animals
Cholesterol biosynthesis
Cholesterol blood
Estrogens analysis
Female
Gene Expression Profiling
Mice
Mice, Knockout
Obesity pathology
Triglycerides biosynthesis
Triglycerides blood
Diet, High-Fat
Histone Demethylases genetics
Intra-Abdominal Fat metabolism
Lipid Metabolism genetics
Obesity genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 9
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 31296899
- Full Text :
- https://doi.org/10.1038/s41598-019-46445-9