Gross Danielle N, Wan Min, Birnbaum Morris J
University of Pennsylvania, School of Medicine, Philadelphia, PA 19104, USA.
Curr Diab Rep. 2009 Jun;9(3):208-14. doi: 10.1007/s11892-009-0034-5.
Forkhead box O (FOXO) transcription factors play an important role in modulating metabolic functions. FOXO is regulated by several modifications, but one of the most critical is phosphorylation and nuclear exclusion by Akt. Given the impact of insulin signaling on Akt-mediated phosphorylation of FOXO and the relatively high expression of Foxo1 in insulin-responsive tissues, this transcription factor is highly poised to regulate energy metabolism. When nutrient and insulin levels are low, Foxo1 promotes expression of gluconeogenic enzymes. Conversely, in the fed state, insulin levels rise and stimulate uptake of glucose primarily into skeletal muscle and other organs, including adipose tissue. Under certain pathophysiologic conditions, including insulin resistance, negative signaling to Foxo1 is compromised. Further clarification of the role of Foxo1 in insulin-responsive tissues will strengthen our understanding and allow us to better combat insulin resistance and diabetes mellitus.
叉头框O(FOXO)转录因子在调节代谢功能中发挥着重要作用。FOXO受多种修饰调控,其中最关键的一种是被Akt磷酸化并排斥于细胞核外。鉴于胰岛素信号对Akt介导的FOXO磷酸化的影响以及Foxo1在胰岛素反应性组织中的相对高表达,该转录因子对调节能量代谢具有高度的调控作用。当营养物质和胰岛素水平较低时,Foxo1促进糖异生酶的表达。相反,在进食状态下,胰岛素水平升高并刺激葡萄糖主要摄取到骨骼肌和其他器官,包括脂肪组织中。在某些病理生理条件下,包括胰岛素抵抗,对Foxo1的负向信号传导受损。进一步阐明Foxo1在胰岛素反应性组织中的作用将加强我们的理解,并使我们能够更好地对抗胰岛素抵抗和糖尿病。