Evidence map›Paper›PMID 31333642›Full record

ReviewFrontiers in immunology2019

The Metabolic Signature of Macrophage Responses.

Antonella Viola, Fabio Munari, Ricardo Sánchez-Rodríguez, Tommaso Scolaro, Alessandra Castegna

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1,264 papers.

0numbers the graph read from it
0cells of the map it votes in
1,264citing papers in PubMed
64.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1,264 citing papers in PubMed, 1,906 citations in OpenAlex.

  1. Trial
  2. Review
  3. New insights into the ACLY-mediated metabolic and epigenetic interplay in macrophages.Journal of enzyme inhibition and medicinal chemistry · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. The Role of Glucose Metabolism inInternational journal of molecular sciences · 2026
    Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

1,204 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Antonella ViolaDepartment of Biomedical Sciences, Istituto di Ricerca Pediatrica, University of Padova, Fondazione Città della Speranza, Padova, Italy.
Fabio MunariDepartment of Biomedical Sciences, Istituto di Ricerca Pediatrica, University of Padova, Fondazione Città della Speranza, Padova, Italy.
Ricardo Sánchez-RodríguezDepartment of Biomedical Sciences, Istituto di Ricerca Pediatrica, University of Padova, Fondazione Città della Speranza, Padova, Italy.
Tommaso ScolaroDepartment of Biomedical Sciences, Istituto di Ricerca Pediatrica, University of Padova, Fondazione Città della Speranza, Padova, Italy.
Alessandra CastegnaDepartment of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari, Bari, Italy.
Città della Speranza Foundation · ITNational Research Council · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophages are a heterogeneous population of immune cells playing several and diverse functions in homeostatic and immune responses. The broad spectrum of macrophage functions depends on both heterogeneity and plasticity of these cells, which are highly specialized in sensing the microenvironment and modify their properties accordingly. Although it is clear that macrophage phenotypes are difficult to categorize and should be seen as plastic and adaptable, they can be simplified into two extremes: a pro-inflammatory (M1) and an anti-inflammatory/pro-resolving (M2) profile. Based on this definition, M1 macrophages are able to start and sustain inflammatory responses, secreting pro-inflammatory cytokines, activating endothelial cells, and inducing the recruitment of other immune cells into the inflamed tissue; on the other hand, M2 macrophages promote the resolution of inflammation, phagocytose apoptotic cells, drive collagen deposition, coordinate tissue integrity, and release anti-inflammatory mediators. Dramatic switches in cell metabolism accompany these phenotypic and functional changes of macrophages. In particular, M1 macrophages rely mainly on glycolysis and present two breaks on the TCA cycle that result in accumulation of itaconate (a microbicide compound) and succinate. Excess of succinate leads to Hypoxia Inducible Factor 1α (HIF1α) stabilization that, in turn, activates the transcription of glycolytic genes, thus sustaining the glycolytic metabolism of M1 macrophages. On the contrary, M2 cells are more dependent on oxidative phosphorylation (OXPHOS), their TCA cycle is intact and provides the substrates for the complexes of the electron transport chain (ETC). Moreover, pro- and anti-inflammatory macrophages are characterized by specific pathways that regulate the metabolism of lipids and amino acids and affect their responses. All these metabolic adaptations are functional to support macrophage activities as well as to sustain their polarization in specific contexts. The aim of this review is to discuss recent findings linking macrophage functions and metabolism.

Indexed as

Macrophage ActivationMacrophagesOxidative PhosphorylationCitric Acid CycleGlycolysisHumansInflammationOxidation-Reductionimmune cross-talkinflammationmacrophagemetabolic rewiringmetabolism

Identifiers

PMID31333642
PMCPMC6618143
OpenAlexW2955084980

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.