Qie Shuo, He Dan, Sang Nianli
Department of Biology, College of Arts and Sciences, Drexel University, Philadelphia, PA, USA.
Department of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC, USA.
Methods Mol Biol. 2019;1928:427-439. doi: 10.1007/978-1-4939-9027-6_22.
Enhanced glutaminolysis and glycolysis are the two most remarkable biochemical features of cancer cell metabolism, reflecting increased utilization of glutamine and glucose in proliferating cells. Most solid tumors often outgrow the blood supply, resulting in a tumor microenvironment characterized by the depletion of glutamine, glucose, and oxygen. Whereas mechanisms by which cancer cells sense and metabolically adapt to hypoxia have been well characterized with a variety of cancer types, mechanisms by which different types of tumor cells respond to a dynamic change of glutamine availability and the underlying importance remains to be characterized. Here we describe the protocol, which uses cultured Hep3B cells as a model in determining glutamine-dependent proliferation, metabolite rescuing, and cellular responses to glutamine depletion. These protocols may be modified to study the metabolic roles of glutamine in other types of tumor or non-tumor cells as well.
增强的谷氨酰胺分解代谢和糖酵解是癌细胞代谢的两个最显著的生化特征,反映了增殖细胞中谷氨酰胺和葡萄糖利用率的增加。大多数实体瘤的生长常常超过血液供应,导致肿瘤微环境的特征是谷氨酰胺、葡萄糖和氧气的消耗。虽然癌细胞感知并代谢适应缺氧的机制在多种癌症类型中已得到充分表征,但不同类型肿瘤细胞对谷氨酰胺可用性动态变化的反应机制及其潜在重要性仍有待表征。在这里,我们描述了该方案,该方案使用培养的Hep3B细胞作为模型来确定谷氨酰胺依赖性增殖、代谢物挽救以及细胞对谷氨酰胺消耗的反应。这些方案也可进行修改,以研究谷氨酰胺在其他类型肿瘤或非肿瘤细胞中的代谢作用。