Nübel Tobias, Emre Yalin, Rabier Daniel, Chadefaux Bernadette, Ricquier Daniel, Bouillaud Frédéric
BIOTRAM, Université Paris Descartes, CNRS UPR9078, Faculté de Médecine Necker-Enfants Malades, 156 rue de Vaugirard 75730 Paris, France.
Biochim Biophys Acta. 2008 Jan;1777(1):48-54. doi: 10.1016/j.bbabio.2007.11.002. Epub 2007 Nov 12.
Uncoupling protein 2 (UCP2) belongs to a family of transporters of the mitochondrial inner membrane and is reported to uncouple respiration from ATP synthesis. Our observation that the amino acid glutamine specifically induces UCP2 protein expression prompted us to investigate metabolic consequences of a UCP2 knockdown (Ucp2-KO) when glutamine is offered as a substrate. We found that Ucp2-KO macrophages incubated in the presence of glutamine exhibit a lower ammonium release, a decreased respiratory rate, and an intracellular accumulation of aspartate. Therefore, we conclude that UCP2 expression is required for efficient oxidation of glutamine in macrophages. This role of UCP2 in glutamine metabolism appears independent from the uncoupling activity of UCP2.
解偶联蛋白2(UCP2)属于线粒体内膜转运蛋白家族,据报道它能使呼吸与ATP合成解偶联。我们观察到氨基酸谷氨酰胺能特异性诱导UCP2蛋白表达,这促使我们研究当以谷氨酰胺为底物时,UCP2基因敲除(Ucp2-KO)的代谢后果。我们发现,在谷氨酰胺存在的情况下培养的Ucp2-KO巨噬细胞铵释放量较低、呼吸速率降低且细胞内天冬氨酸积累。因此,我们得出结论,巨噬细胞中谷氨酰胺的有效氧化需要UCP2表达。UCP2在谷氨酰胺代谢中的这一作用似乎独立于UCP2的解偶联活性。