Molecular Nutritional Medicine, Technische Universität München, Else Kröner-Fresenius-Zentrum (EKFZ) & Research Center for Nutrition and Food Sciences (ZIEL), Gregor-Mendel-Str. 2, 85350 Freising-Weihenstephan, Germany.
Heinrich-Heine-Universität Düsseldorf, Molecular Proteomics Laboratory, BMFZ, Universitätsstr. 1, 40225 Düsseldorf, Germany.
J Nutr Biochem. 2015 Jan;26(1):75-81. doi: 10.1016/j.jnutbio.2014.09.002. Epub 2014 Oct 2.
DJ-1 constitutes a ubiquitously expressed, oxidative stress-responsive protein with multiple functions. DJ-1 emerged as a candidate from our previous proteome analysis investigating alterations in the hypothalamus in three mouse strains differing in their susceptibility to diet-induced obesity (DIO). Validation studies demonstrated a high-fat diet (HFD)-induced shift in the DJ-1 isoform pattern in the hypothalamus and several other tissues of mice. Others found HFD-induced alterations in DJ-1 protein abundance in adipose tissue and pancreatic islets in wild-type rodents. Here, we investigated the gene-diet interaction by challenging Dj-1(-/-) mice with a HFD. We demonstrate that the development of diet-induced obesity (DIO) Dj-1(-/-) mice is according to wild-type mice with the exception of transient higher gains in fat mass at the expense of lean mass after 14 weeks of feeding.
DJ-1 是一种广泛表达的、对氧化应激有反应的蛋白质,具有多种功能。DJ-1 是从我们之前的蛋白质组分析中作为候选物出现的,该分析研究了三种对饮食诱导肥胖(DIO)易感性不同的小鼠品系下丘脑的变化。验证研究表明,高脂肪饮食(HFD)诱导了小鼠下丘脑和其他几种组织中 DJ-1 同工型模式的改变。其他人发现,在野生型啮齿动物的脂肪组织和胰岛中,HFD 诱导 DJ-1 蛋白丰度发生变化。在这里,我们通过用 HFD 挑战 Dj-1(-/-) 小鼠来研究基因-饮食相互作用。我们证明,除了在喂养 14 周后以瘦体重为代价短暂增加脂肪量外,DIO Dj-1(-/-) 小鼠的发展与野生型小鼠一致。