Department of Biochemistry & Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
FASEB J. 2021 Jul;35(7):e21728. doi: 10.1096/fj.202100381RR.
Proliferation and differentiation of preadipocytes, and other cell types, is accompanied by an increase in glucose uptake. Previous work showed that a pulse of high glucose was required during the first 3 days of differentiation in vitro, but was not required after that. The specific glucose metabolism pathways required for adipocyte differentiation are unknown. Herein, we used 3T3-L1 adipocytes as a model system to study glucose metabolism and expansion of the adipocyte metabolome during the first 3 days of differentiation. Our primary outcome measures were GLUT4 and adiponectin, key proteins associated with healthy adipocytes. Using complete media with 0 or 5 mM glucose, we distinguished between developmental features that were dependent on the differentiation cocktail of dexamethasone, insulin, and isobutylmethylxanthine alone or the cocktail plus glucose. Cocktail alone was sufficient to activate the capacity for 2-deoxglucose uptake and glycolysis, but was unable to support the expression of GLUT4 and adiponectin in mature adipocytes. In contrast, 5 mM glucose in the media promoted a transient increase in glucose uptake and glycolysis as well as a significant expansion of the adipocyte metabolome and proteome. Using genetic and pharmacologic approaches, we found that the positive effects of 5 mM glucose on adipocyte differentiation were specifically due to increased expression of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 3 (PFKFB3), a key regulator of glycolysis and the ancillary glucose metabolic pathways. Our data reveal a critical role for PFKFB3 activity in regulating the cellular metabolic remodeling required for adipocyte differentiation and maturation.
前脂肪细胞和其他细胞类型的增殖和分化伴随着葡萄糖摄取的增加。先前的工作表明,在体外分化的前 3 天需要一个高葡萄糖脉冲,但此后不需要。脂肪细胞分化所需的特定葡萄糖代谢途径尚不清楚。在此,我们使用 3T3-L1 脂肪细胞作为模型系统,研究了在分化的前 3 天内葡萄糖代谢和脂肪细胞代谢组的扩张。我们的主要结果测量指标是 GLUT4 和脂联素,这是与健康脂肪细胞相关的关键蛋白。使用含有 0 或 5mM 葡萄糖的完全培养基,我们区分了依赖于地塞米松、胰岛素和异丁基甲基黄嘌呤分化鸡尾酒本身或鸡尾酒加葡萄糖的发育特征。单独的鸡尾酒足以激活 2-脱氧葡萄糖摄取和糖酵解的能力,但无法支持成熟脂肪细胞中 GLUT4 和脂联素的表达。相比之下,培养基中的 5mM 葡萄糖促进了葡萄糖摄取和糖酵解的短暂增加,以及脂肪细胞代谢组和蛋白质组的显著扩张。通过遗传和药理学方法,我们发现 5mM 葡萄糖对脂肪细胞分化的积极影响是由于 6-磷酸果糖-2-激酶/果糖-2,6-双磷酸酶 3(PFKFB3)的表达增加所致,PFKFB3 是糖酵解和辅助葡萄糖代谢途径的关键调节剂。我们的数据揭示了 PFKFB3 活性在调节脂肪细胞分化和成熟所需的细胞代谢重编程中的关键作用。