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