Dai Wenting, Jiang Lei
Department of Molecular and Cellular Endocrinology, Diabetes and Metabolism Research Institute, Duarte, CA, United States.
Comprehensive Cancer Center, City of Hope Medical Center, Duarte, CA, United States.
Front Endocrinol (Lausanne). 2019 Sep 3;10:570. doi: 10.3389/fendo.2019.00570. eCollection 2019.
Metabolism describes the life-sustaining chemical reactions in organisms that provide both energy and building blocks for cellular survival and proliferation. Dysregulated metabolism leads to many life-threatening diseases including obesity, diabetes, and cancer. Mitochondria, subcellular organelles, contain the central energy-producing metabolic pathway, the tricarboxylic acid (TCA) cycle. Also, mitochondria exist in a dynamic network orchestrated by extracellular nutrient levels and intracellular energy needs. Upon stimulation, mitochondria undergo consistent interchange through fusion (small to big) and fission (big to small) processes. Mitochondrial fusion is primarily controlled by three GTPases, mitofusin 1 (Mfn1), Mfn2, and optic atrophy 1 (Opa1), while mitochondrial fission is primarily regulated by GTPase dynamin-related protein 1 (Drp1). Dysregulated activity of these GTPases results in disrupted mitochondrial dynamics and cellular metabolism. This review will update the metabolic roles of these GTPases in obesity, diabetes, and cancer.
新陈代谢描述了生物体中维持生命的化学反应,这些反应为细胞的存活和增殖提供能量和构建模块。新陈代谢失调会导致许多危及生命的疾病,包括肥胖症、糖尿病和癌症。线粒体作为亚细胞器,包含产生能量的核心代谢途径——三羧酸(TCA)循环。此外,线粒体存在于一个由细胞外营养水平和细胞内能量需求精心调控的动态网络中。受到刺激时,线粒体通过融合(由小变大)和裂变(由大变小)过程持续进行相互转换。线粒体融合主要由三种GTP酶,即线粒体融合蛋白1(Mfn1)、Mfn2和视神经萎缩蛋白1(Opa1)控制,而线粒体裂变主要由GTP酶动力相关蛋白1(Drp1)调节。这些GTP酶的活性失调会导致线粒体动态变化和细胞代谢紊乱。本综述将更新这些GTP酶在肥胖症、糖尿病和癌症中的代谢作用。