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脂肪量和肥胖相关基因Fto影响小鼠白色脂肪组织的饮食反应。

Fat mass- and obesity-associated gene Fto affects the dietary response in mouse white adipose tissue.

作者信息

Ronkainen Justiina, Huusko Tuija J, Soininen Raija, Mondini Eleonora, Cinti Francesca, Mäkelä Kari A, Kovalainen Miia, Herzig Karl-Heinz, Järvelin Marjo-Riitta, Sebert Sylvain, Savolainen Markku J, Salonurmi Tuire

机构信息

1] Biocenter Oulu, University of Oulu, Oulu, Finland [2] Institute of Clinical Medicine, Department of Internal Medicine, University of Oulu, Oulu, Finland [3] Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland.

1] Biocenter Oulu, University of Oulu, Oulu, Finland [2] Faculty of Biochemistry and Molecular Medicine, Oulu Center for Cell-Matrix Research, University of Oulu, Oulu, Finland.

出版信息

Sci Rep. 2015 Mar 18;5:9233. doi: 10.1038/srep09233.

Abstract

Common variants of human fat mass- and obesity-associated gene Fto have been linked with higher body mass index, but the biological explanation for the link has remained obscure. Recent findings suggest that these variants affect the homeobox protein IRX3. Here we report that FTO has a role in white adipose tissue which modifies its response to high-fat feeding. Wild type and Fto-deficient mice were exposed to standard or high-fat diet for 16 weeks after which metabolism, behavior and white adipose tissue morphology were analyzed together with adipokine levels and relative expression of genes regulating white adipose tissue adipogenesis and Irx3. Our results indicate that Fto deficiency increases the expression of genes related to adipogenesis preventing adipocytes from becoming hypertrophic after high-fat diet. In addition, we report a novel finding of increased Irx3 expression in Fto-deficient mice after high-fat feeding indicating a complex link between FTO, IRX3 and fat metabolism.

摘要

人类脂肪量和肥胖相关基因Fto的常见变体与较高的体重指数有关,但这种关联的生物学解释仍不清楚。最近的研究结果表明,这些变体影响同源框蛋白IRX3。在此我们报告,FTO在白色脂肪组织中发挥作用,可改变其对高脂喂养的反应。将野生型和Fto基因缺陷型小鼠暴露于标准饮食或高脂饮食16周,之后分析其代谢、行为和白色脂肪组织形态,同时检测脂肪因子水平以及调节白色脂肪组织脂肪生成的基因和Irx3的相对表达。我们的结果表明,Fto基因缺陷会增加与脂肪生成相关的基因表达,从而防止高脂饮食后脂肪细胞肥大。此外,我们报告了一项新发现,即高脂喂养后Fto基因缺陷型小鼠中Irx3表达增加,这表明FTO、IRX3与脂肪代谢之间存在复杂的联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55e7/4363842/1612eb71397f/srep09233-f1.jpg

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