Evidence map›Paper›PMID 28340958›Full record

ReviewSeminars in immunology2016

Metabolism and acetylation in innate immune cell function and fate.

Alanna M Cameron, Simon J Lawless, Edward J Pearce

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

35 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
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  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Molecular autism · 2024
    Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. A guide to interrogating immunometabolism.Nature reviews. Immunology · 2021
    Review
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

3 authors at 2 institutions in 1 country.

Alanna M CameronDepartment of Immunometabolism, Max Planck Institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany.
Simon J LawlessDepartment of Immunometabolism, Max Planck Institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany.
Edward J PearceDepartment of Immunometabolism, Max Planck Institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany; Faculty of Biology, University of Freiburg, 79104 Freiburg, Germany. Electronic address: pearceed@ie-freiburg.mpg.de.
Max Planck Institute of Immunobiology and Epigenetics · DEUniversity of Freiburg · DE

Funding

SCHISTOSOME EGG-INDUCED TH2 RESPONSESR01AI032573 · NIAID · WASHINGTON UNIVERSITY · PI PEARCE, EDWARD J. · 1993 to 2016
$5.4M
Dendritic Cell Function in SchistosomiasisR01AI053825 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI PEARCE, EDWARD J. · 2002 to 2010
$3.4M
MANIPULATING DENDRITIC CELL METABOLISM TO PROMOTE CANCER IMMUNITYR01CA164062 · NCI · WASHINGTON UNIVERSITY · PI PEARCE, EDWARD J. · 2012 to 2016
$1.7M
MACROPHAGE FATTY ACID METABOLISM IN IMMUNITY TO HELMINTHSR01AI110481 · NIAID · WASHINGTON UNIVERSITY · PI PEARCE, EDWARD J. · 2015 to 2019
$1.5M
Schistosome egg induced TH2 responsesR56AI032573 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI PEARCE, EDWARD J. · 2007 to 2007
$394k
NCI NIH HHS R01 CA164062NIAID NIH HHS R01 AI032573NIAID NIH HHS R01 AI053825NIAID NIH HHS R01 AI110481NIAID NIH HHS R56 AI032573
6 · The paper itself

Abstract

Innate immunity is the first line of defense against invading pathogens. Changes in both metabolism and chromatin accessibility contribute to the shaping of these innate immune responses, and we are beginning to appreciate that cross-talk between these two systems plays an important role in determining innate immune cell differentiation and function. In this review we focus on acetylation, a post-translational modification important for both regulating chromatin accessibility by modulating histone function, and for functional regulation of non-histone proteins, which has many links to both immune signaling and metabolism. We discuss the interactions between metabolism and acetylation, including the requirement for metabolic intermediates as substrates and co-factors for acetylation, and the regulation of metabolic proteins and enzymes by acetylation. Here we highlight recent findings, which demonstrate the role that the metabolism-acetylation axis has in coordinating the responses of innate immune cells to the availability of nutrients and the microenvironment.

Indexed as

Energy MetabolismImmunity, InnateAcetylationAnimalsEpigenesis, GeneticGene Expression RegulationHistonesHumansImmune SystemImmunomodulationSignal TransductionHistonesAcetylationDendritic cellsImmunometabolismInnate immunityMacrophages

Identifiers

PMID28340958
PMCPMC10911065
OpenAlexW2542928920

What OpenQuestion holds

Textmetadata
LicenceTDM
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.