Evidence map›Paper›PMID 26485286›Full record

ArticleThe Journal of clinical investigation2015

High salt reduces the activation of IL-4- and IL-13-stimulated macrophages.

Katrina J Binger, Matthias Gebhardt, Matthias Heinig, Carola Rintisch, Agnes Schroeder, Wolfgang Neuhofer, Karl Hilgers, Arndt Manzel, Christian Schwartz, Markus Kleinewietfeld and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 172 papers.

0numbers the graph read from it
0cells of the map it votes in
172citing papers in PubMed
21.2field-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

172 citing papers in PubMed, 274 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Salt and chronic kidney disease.Nature reviews. Nephrology · 2026
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Aging and sex differences in salt sensitivity of blood pressure.Clinical science (London, England : 1979) · 2025
    Review
  17. Metal Ion Signaling in Biomedicine.Chemical reviews · 2025
    Review
  18. Article
  19. Review
  20. Review

112 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 7 institutions in 3 countries.

Katrina J Binger
Matthias Gebhardt
Matthias Heinig
Carola Rintisch
Agnes Schroeder
Wolfgang Neuhofer
Karl Hilgers
Arndt Manzel
Christian Schwartz
Markus Kleinewietfeld
Jakob Voelkl
Valentin Schatz
Ralf A Linker
Florian Lang
David Voehringer
Mark D Wright
Norbert Hubner
Ralf Dechend
Jonathan Jantsch
Jens Titze
Dominik N Müller
Max Delbrück Center · DEUniversitätsklinikum Erlangen · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DEUniversity Hospital Regensburg · DEUniversity of Tübingen · DEHelios Hospital Berlin-Buch · DEMonash University · AU

Funding

Lymphatic Regulation of Skin Electrolyte Metabolism and Blood PressureR01HL118579 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI TITZE, JENS MARC · 2013 to 2017
$1.9M
NHLBI NIH HHS R01 HL118579NHLBI NIH HHS R01 HL118579-01
6 · The paper itself

Abstract

A high intake of dietary salt (NaCl) has been implicated in the development of hypertension, chronic inflammation, and autoimmune diseases. We have recently shown that salt has a proinflammatory effect and boosts the activation of Th17 cells and the activation of classical, LPS-induced macrophages (M1). Here, we examined how the activation of alternative (M2) macrophages is affected by salt. In stark contrast to Th17 cells and M1 macrophages, high salt blunted the alternative activation of BM-derived mouse macrophages stimulated with IL-4 and IL-13, M(IL-4+IL-13) macrophages. Salt-induced reduction of M(IL-4+IL-13) activation was not associated with increased polarization toward a proinflammatory M1 phenotype. In vitro, high salt decreased the ability of M(IL-4+IL-13) macrophages to suppress effector T cell proliferation. Moreover, mice fed a high salt diet exhibited reduced M2 activation following chitin injection and delayed wound healing compared with control animals. We further identified a high salt-induced reduction in glycolysis and mitochondrial metabolic output, coupled with blunted AKT and mTOR signaling, which indicates a mechanism by which NaCl inhibits full M2 macrophage activation. Collectively, this study provides evidence that high salt reduces noninflammatory innate immune cell activation and may thus lead to an overall imbalance in immune homeostasis.

Indexed as

AnimalsBone Marrow CellsCells, CulturedChitinGene Expression RegulationGlycolysisHistone CodeImmunity, InnateInflammationInterleukin-13Interleukin-4Macrophage ActivationMacrophagesMaleMiceMice, Inbred C57BLAkt1 protein, mouseChitinInterleukin-13Interleukin-4mTOR protein, mouseProto-Oncogene Proteins c-aktSodium ChlorideSodium Chloride, DietaryTOR Serine-Threonine Kinases

Identifiers

PMID26485286
PMCPMC4639967
OpenAlexW2139654366

What OpenQuestion holds

Textmetadata
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.