Glycolytic Stimulation Is Not a Requirement for M2 Macrophage Differentiation

Feilong Wang, Song Zhang, Ivan Vuckovic, Ryounghoon Jeon, Amir Lerman, Clifford D. Folmes, Petras P. Dzeja, Joerg Herrmann

Research output: Contribution to journalArticlepeer-review

46 Scopus citations

Abstract

Enhanced glucose uptake and a switch to glycolysis are key traits of M1 macrophages, whereas enhanced fatty acid oxidation and oxidative phosphorylation are the main metabolic characteristics of M2 macrophages. Recent studies challenge this traditional view, indicating that glycolysis may also be critically important for M2 macrophage differentiation, based on experiments with 2-DG. Here we confirm the inhibitory effect of 2-DG on glycolysis, but also demonstrate that 2-DG impairs oxidative phosphorylation and significantly reduces 13C-labeled Krebs cycle metabolites and intracellular ATP levels. These metabolic derangements were associated with reduced JAK-STAT6 pathway activity and M2 differentiation marker expression. While glucose deprivation and glucose substitution with galactose effectively suppressed glycolytic activity, there was no effective suppression of oxidative phosphorylation, intracellular ATP levels, STAT6 phosphorylation, and M2 differentiation marker expression. These data indicate that glycolytic stimulation is not required for M2 macrophage differentiation as long as oxidative phosphorylation remains active. Wang et al. reassess the role of glycolysis in alternatively activated (M2) macrophages and find that glucose depletion, leaving OXPHOS intact, does not affect M2 activation. However, the glucose analog 2-DG, which impairs both glycolysis and OXPHOS, and reduces intracellular ATP and JAK-STAT6 signaling, impairs M2 differentiation.

Original languageEnglish (US)
Pages (from-to)463-475.e4
JournalCell Metabolism
Volume28
Issue number3
DOIs
StatePublished - Sep 4 2018

Keywords

  • 2-DG
  • M2 macrophage
  • alternative stimulation
  • glucose
  • glycolysis
  • interleukin-4
  • metabolism

ASJC Scopus subject areas

  • Physiology
  • Molecular Biology
  • Cell Biology

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