首页    期刊浏览 2024年12月02日 星期一
登录注册

文章基本信息

  • 标题:Murine double minute 2 aggravates adipose tissue dysfunction through ubiquitin-mediated six-transmembrane epithelial antigen of prostate 4 degradation
  • 本地全文:下载
  • 作者:Wei Zhao ; Qiang Xu ; Jiahui Yang
  • 期刊名称:iScience
  • 印刷版ISSN:2589-0042
  • 出版年度:2022
  • 卷号:25
  • 期号:7
  • 页码:1-22
  • DOI:10.1016/j.isci.2022.104544
  • 语种:English
  • 出版社:Elsevier
  • 摘要:SummaryHealthy adipose tissue is crucial to maintain normal energy homeostasis. Little is known about the role of murine double minute 2 (MDM2), an E3 ubiquitin ligase and has been highlighted in oncopathology, in adipose tissue. Our results indicated that MDM2 expression was associated with nutritional status.Mdm2adipocyte-specific knock-in (Mdm2-AKI) mice exhibited exacerbated weight gain, insulin resistance, and decreased energy expenditure. Meanwhile, chronic high-fat diet (HFD) exposure caused obvious epididymal white adipose tissue (eWAT) dysfunction, such as senescence, apoptosis, and chronic inflammation, thereby leading to hepatic steatosis inMdm2-AKI mice. Mechanically, MDM2 could interact with six-transmembrane epithelial antigen of prostate 4 (STEAP4) and inhibit STEAP4 expression through ubiquitin-mediated STEAP4 degradation. Thereinto, the K18 and K161 sites of STEAP4 were ubiquitin-modificated by MDM2. Finally, STEAP4 restoration in eWAT ofMdm2-AKI mice on a HFD rescued MDM2-induced adipose dysfunction, insulin resistance, and hepatic steatosis. Summary, the MDM2-STEAP4 axis in eWAT plays an important role in maintaining healthy adipose tissue function and improving hepatic steatosis.Graphical abstractDisplay OmittedHighlights•Murine double minute 2 (MDM2) overexpression intensifies high-fat diet-induced adipose tissue dysfunction•Adipocyte MDM2 overexpression aggravates insulin resistance and hepatosteatosis•MDM2 decreases six-transmembrane epithelial antigen of prostate 4 (STEAP4) expression by ubiquitin-dependent STEAP4 degradation•STEAP4 overexpression in eWAT alleviates MDM2-induced metabolic disorderBiological sciences; Molecular biology; Immunology; Proteomics
国家哲学社会科学文献中心版权所有