| Literature DB >> 29262332 |
James R Krycer1, Katsuyuki Yugi2, Akiyoshi Hirayama3, Daniel J Fazakerley1, Lake-Ee Quek4, Richard Scalzo5, Satoshi Ohno6, Mark P Hodson7, Satsuki Ikeda8, Futaba Shoji8, Kumi Suzuki8, Westa Domanova9, Benjamin L Parker1, Marin E Nelson1, Sean J Humphrey1, Nigel Turner10, Kyle L Hoehn11, Gregory J Cooney12, Tomoyoshi Soga3, Shinya Kuroda13, David E James14.
Abstract
Insulin triggers an extensive signaling cascade to coordinate adipocyte glucose metabolism. It is considered that the major role of insulin is to provide anabolic substrates by activating GLUT4-dependent glucose uptake. However, insulin stimulates phosphorylation of many metabolic proteins. To examine the implications of this on glucose metabolism, we performed dynamic tracer metabolomics in cultured adipocytes treated with insulin. Temporal analysis of metabolite concentrations and tracer labeling revealed rapid and distinct changes in glucose metabolism, favoring specific glycolytic branch points and pyruvate anaplerosis. Integrating dynamic metabolomics and phosphoproteomics data revealed that insulin-dependent phosphorylation of anabolic enzymes occurred prior to substrate accumulation. Indeed, glycogen synthesis was activated independently of glucose supply. We refer to this phenomenon as metabolic priming, whereby insulin signaling creates a demand-driven system to "pull" glucose into specific anabolic pathways. This complements the supply-driven regulation of anabolism by substrate accumulation and highlights an additional role for insulin action in adipocyte glucose metabolism.Entities:
Keywords: adipocyte; glucose; insulin; metabolic priming; metabolic tracer; metabolomics
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Year: 2017 PMID: 29262332 DOI: 10.1016/j.celrep.2017.11.085
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423