首页    期刊浏览 2024年12月01日 星期日
登录注册

文章基本信息

  • 标题:Disruption of tumor suppressor gene Hint1 leads to remodeling of the lipid metabolic phenotype of mouse liver
  • 本地全文:下载
  • 作者:Diren Beyoğlu ; Kristopher W. Krausz ; Juliette Martin
  • 期刊名称:JLR Papers In Press
  • 印刷版ISSN:0022-2275
  • 电子版ISSN:1539-7262
  • 出版年度:2014
  • 卷号:55
  • 期号:11
  • 页码:2309-2319
  • DOI:10.1194/jlr.M050682
  • 语种:English
  • 出版社:American Society for Biochemistry and Molecular Biology
  • 摘要:A lipidomic and metabolomic investigation of serum and liver from mice was performed to gain insight into the tumor suppressor gene Hint1 . A major reprogramming of lipid homeostasis was found in both serum and liver of Hint1 -null ( Hint −/−) mice, with significant changes in the levels of many lipid molecules, as compared with gender-, age-, and strain-matched WT mice. In the Hint1 −/− mice, serum total and esterified cholesterol were reduced 2.5-fold, and lysophosphatidylcholines (LPCs) and lysophosphatidic acids were 10-fold elevated in serum, with a corresponding fall in phosphatidylcholines (PCs). In the liver, MUFAs and PUFAs, including arachidonic acid (AA) and its metabolic precursors, were also raised, as was mRNA encoding enzymes involved in AA de novo synthesis. There was also a significant 50% increase in hepatic macrophages in the Hint1 −/− mice. Several hepatic ceramides and acylcarnitines were decreased in the livers of Hint1 −/− mice. The changes in serum LPCs and PCs were neither related to hepatic phospholipase A2 activity nor to mRNAs encoding lysophosphatidylcholine acetyltransferases 1-4. The lipidomic phenotype of the Hint1 −/− mouse revealed decreased inflammatory eicosanoids with elevated proliferative mediators that, combined with decreased ceramide apoptosis signaling molecules, may contribute to the tumor suppressor activity of Hint1 .
  • 关键词:lipidomics ; metabolomics ; mass spectrometry ; carcinogenesis ; cholesterol ; phospholipids ; eicosanoids ; proliferation ; apoptosis
国家哲学社会科学文献中心版权所有