Chair of Molecular Nutritional Medicine, TUM School of Life Sciences, Technical University of Munich, Germany; EKFZ - Else Kröner-Fresenius Center for Nutritional Medicine, Technical University of Munich, Freising, Germany; ZIEL - Institute for Food & Health, Technical University of Munich, Freising, Germany.
Bavarian Center for Biomolecular Mass Spectrometry (BayBioMS), Technical University of Munich, Freising, Germany.
Mol Metab. 2018 Feb;8:77-85. doi: 10.1016/j.molmet.2017.12.010. Epub 2017 Dec 26.
Non-shivering thermogenesis in mammalian brown adipose tissue depends on thermogenic uncoupling protein 1. Its activity is triggered by free fatty acids while purine nucleotides mediate inhibition. During activation, it is thought that free fatty acids overcome purine-mediated inhibition. We measured the cellular concentration and the release of purine nucleotide metabolites to uncover a possible role of purine nucleotide degradation in uncoupling protein 1 activation.
With mass spectrometry, purine nucleotide metabolites were quantified in cellular homogenates and supernatants of cultured primary brown adipocytes. We also determined oxygen consumption in response to a β-adrenergic agonist.
Upon adrenergic activation, brown adipocytes decreased the intracellular concentration of inhibitory nucleotides (ATP, ADP, GTP and GDP) and released the respective degradation products. At the same time, an increase in cellular calcium occurred. None of these phenomena occurred in white adipocytes or myotubes. The brown adipocyte expression of enzymes implicated in purine metabolic remodeling is altered upon cold exposure. Pharmacological and genetic interference of purine metabolism altered uncoupling protein 1 mediated uncoupled respiration.
Adrenergic stimulation of brown adipocytes lowers the intracellular concentration of purine nucleotides, thereby contributing to uncoupling protein 1 activation.
哺乳动物棕色脂肪组织的非颤抖性产热依赖于解偶联蛋白 1。其活性受游离脂肪酸触发,而嘌呤核苷酸介导抑制。在激活过程中,人们认为游离脂肪酸克服了嘌呤介导的抑制。我们测量了细胞内浓度和嘌呤核苷酸代谢物的释放,以揭示嘌呤核苷酸降解在解偶联蛋白 1 激活中的可能作用。
用质谱法定量培养原代棕色脂肪细胞的细胞匀浆和上清液中的嘌呤核苷酸代谢物。我们还测定了对β-肾上腺素激动剂的耗氧量。
在肾上腺素激活后,棕色脂肪细胞降低了抑制性核苷酸(ATP、ADP、GTP 和 GDP)的细胞内浓度,并释放了各自的降解产物。同时,细胞内钙增加。这些现象均未发生在白色脂肪细胞或肌管中。冷暴露会改变棕色脂肪细胞中参与嘌呤代谢重塑的酶的表达。嘌呤代谢的药理学和遗传学干扰改变了解偶联蛋白 1 介导的解偶联呼吸。
肾上腺素刺激棕色脂肪细胞降低细胞内嘌呤核苷酸浓度,从而有助于解偶联蛋白 1 的激活。