Park Yoon Jeong, Choe Sung Sik, Sohn Jee Hyung, Kim Jae Bum
a Department of Biological Science , Institute of Molecular Biology & Genetics, Seoul National University , Seoul , Korea.
b Department of Biophysics and Chemical Biology , Seoul National University , Seoul , Korea.
Adipocyte. 2017 Apr 3;6(2):147-153. doi: 10.1080/21623945.2017.1288321. Epub 2017 Feb 8.
Obesity is closely associated with metabolic diseases including type 2 diabetes. One hallmark characteristics of obesity is chronic inflammation that is coordinately controlled by complex signaling networks in adipose tissues. Compelling evidence indicates that reactive oxygen species (ROS) and its related signaling pathways play crucial roles in the progression of chronic inflammation in obesity. The pentose phosphate pathway (PPP) is an anabolic pathway that utilizes the glucoses to generate molecular building blocks and reducing equivalents in the form of NADPH. In particular, NADPH acts as one of the key modulators in the control of ROS through providing an electron for both ROS generation and scavenging. Recently, we have reported that glucose-6-phosphate dehydrogenase (G6PD), a rate-limiting enzyme of the PPP, is implicated in adipose tissue inflammation and systemic insulin resistance in obesity. Mechanistically, G6PD potentiates generation of ROS that augments pro-inflammatory responses in adipose tissue macrophages, leading to systemic insulin resistance. Here, we provide an overview of cell type- specific roles of G6PD in the regulation of ROS balance as well as additional details on the significance of G6PD that contributes to pro-oxidant NADPH generation in obesity-related chronic inflammation and insulin resistance.
肥胖与包括2型糖尿病在内的代谢性疾病密切相关。肥胖的一个标志性特征是慢性炎症,它由脂肪组织中的复杂信号网络协同控制。有力证据表明,活性氧(ROS)及其相关信号通路在肥胖相关慢性炎症的进展中起关键作用。磷酸戊糖途径(PPP)是一种合成代谢途径,利用葡萄糖生成分子构件并以NADPH的形式产生还原当量。特别是,NADPH通过为ROS的产生和清除提供电子,作为控制ROS的关键调节因子之一。最近,我们报道了PPP的限速酶葡萄糖-6-磷酸脱氢酶(G6PD)与肥胖中的脂肪组织炎症和全身胰岛素抵抗有关。从机制上讲,G6PD增强ROS的产生,从而增强脂肪组织巨噬细胞中的促炎反应,导致全身胰岛素抵抗。在这里,我们概述了G6PD在调节ROS平衡中的细胞类型特异性作用,以及G6PD在肥胖相关慢性炎症和胰岛素抵抗中促进促氧化NADPH生成的重要性的更多细节。