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本文引用的文献

1
A Complex Relationship between Immunity and Metabolism in Drosophila Diet-Induced Insulin Resistance.果蝇饮食诱导胰岛素抵抗中免疫与代谢之间的复杂关系。
Mol Cell Biol. 2017 Dec 29;38(2). doi: 10.1128/MCB.00259-17. Print 2018 Jan 15.
2
The cold-induced lipokine 12,13-diHOME promotes fatty acid transport into brown adipose tissue.冷诱导脂肪因子12,13-二羟基十八碳二烯酸促进脂肪酸转运至棕色脂肪组织。
Nat Med. 2017 May;23(5):631-637. doi: 10.1038/nm.4297. Epub 2017 Mar 27.
3
Inflammation, metaflammation and immunometabolic disorders.炎症、代谢性炎症和免疫代谢紊乱。
Nature. 2017 Feb 8;542(7640):177-185. doi: 10.1038/nature21363.
4
Genetic Screen in Drosophila Larvae Links ird1 Function to Toll Signaling in the Fat Body and Hemocyte Motility.果蝇幼虫的遗传筛选将ird1功能与脂肪体中的Toll信号传导及血细胞运动联系起来。
PLoS One. 2016 Jul 28;11(7):e0159473. doi: 10.1371/journal.pone.0159473. eCollection 2016.
5
Effects of exercise training on intrahepatic lipid content in humans.运动训练对人体肝脏内脂质含量的影响。
Diabetologia. 2016 Oct;59(10):2068-79. doi: 10.1007/s00125-016-4037-x. Epub 2016 Jul 8.
6
Tissue communication in a systemic immune response of Drosophila.果蝇全身免疫反应中的组织通讯。
Fly (Austin). 2016 Jul 2;10(3):115-22. doi: 10.1080/19336934.2016.1182269. Epub 2016 Apr 26.
7
The canonical Wingless signaling pathway is required but not sufficient for inflow tract formation in the Drosophila melanogaster heart.经典的无翅信号通路对于黑腹果蝇心脏流入道的形成是必需的,但并不充分。
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8
CoA protects against the deleterious effects of caloric overload in Drosophila.辅酶A可保护果蝇免受热量过载的有害影响。
J Lipid Res. 2016 Mar;57(3):380-7. doi: 10.1194/jlr.M062976. Epub 2016 Jan 24.
9
Ecdysone Titer Determined by 3DE-3β-Reductase Enhances the Immune Response in the Silkworm.由3DE - 3β - 还原酶测定的蜕皮激素滴度增强家蚕的免疫反应。
J Immunol. 2016 Feb 15;196(4):1646-54. doi: 10.4049/jimmunol.1500158. Epub 2016 Jan 15.
10
The Anti-Adipogenic Potential of COUP-TFII Is Mediated by Downregulation of the Notch Target Gene Hey1.COUP-TFII的抗脂肪生成潜能是通过Notch靶基因Hey1的下调介导的。
PLoS One. 2015 Dec 31;10(12):e0145608. doi: 10.1371/journal.pone.0145608. eCollection 2015.

七喜是胰岛素信号的新型调节剂。

Seven-Up Is a Novel Regulator of Insulin Signaling.

机构信息

Division of Endocrinology, Metabolism, and Lipid Research, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri 63110

Department of Biological Sciences, Binghamton University, New York 13902.

出版信息

Genetics. 2018 Apr;208(4):1643-1656. doi: 10.1534/genetics.118.300770. Epub 2018 Feb 27.

DOI:10.1534/genetics.118.300770
PMID:29487137
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5887154/
Abstract

Insulin resistance is associated with obesity, cardiovascular disease, non-alcoholic fatty liver disease, and type 2 diabetes. These complications are exacerbated by a high-calorie diet, which we used to model type 2 diabetes in Our studies focused on the fat body, an adipose- and liver-like tissue that stores fat and maintains circulating glucose. A gene regulatory network was constructed to predict potential regulators of insulin signaling in this tissue. Genomic characterization of fat bodies suggested a central role for the transcription factor Seven-up (Svp). Here, we describe a new role for Svp as a positive regulator of insulin signaling. Tissue-specific loss-of-function showed that Svp is required in the fat body to promote glucose clearance, lipid turnover, and insulin signaling. Svp appears to promote insulin signaling, at least in part, by inhibiting ecdysone signaling. Svp also impairs the immune response possibly via inhibition of antimicrobial peptide expression in the fat body. Taken together, these studies show that gene regulatory networks can help identify positive regulators of insulin signaling and metabolic homeostasis using the fat body.

摘要

胰岛素抵抗与肥胖、心血管疾病、非酒精性脂肪肝和 2 型糖尿病有关。这些并发症会因高热量饮食而加重,我们曾用这种饮食来模拟 2 型糖尿病。我们的研究集中在脂肪组织上,脂肪组织是一种具有脂肪和肝脏样功能的组织,可储存脂肪并维持循环葡萄糖。构建了一个基因调控网络,以预测该组织中胰岛素信号的潜在调节剂。脂肪组织的基因组特征表明转录因子 Seven-up (Svp) 具有核心作用。在这里,我们描述了 Svp 作为胰岛素信号的正调控因子的新作用。组织特异性功能丧失表明,Svp 在脂肪组织中是必需的,以促进葡萄糖清除、脂质周转和胰岛素信号。Svp 似乎通过抑制蜕皮激素信号来促进胰岛素信号,至少在一定程度上是这样。Svp 还可能通过抑制脂肪体中抗菌肽的表达来损害免疫反应。总之,这些研究表明,使用脂肪体,基因调控网络可以帮助识别胰岛素信号和代谢稳态的正调节剂。