Evidence map›Paper›PMID 31160535›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2019

Lactic Acid Inhibits Lipopolysaccharide-Induced Mast Cell Function by Limiting Glycolysis and ATP Availability.

Heather L Caslin, Daniel Abebayehu, Amina Abdul Qayum, Tamara T Haque, Marcela T Taruselli, Patrick A Paez, Neha Pondicherry, Brian O Barnstein, L Alexis Hoeferlin, Charles E Chalfant and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

56 citing papers in PubMed, 72 citations in OpenAlex.

  1. Review
  2. The role of lactate in retinal health and disease: mechanisms and potential therapeutic strategies. A narrative review.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2026
    Review
  3. Article
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  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Journal of inflammation research · 2026
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Lactate in Anaphylaxis: 100 Years On.Sports medicine (Auckland, N.Z.) · 2025
    Review
  17. Article
  18. Review
  19. Review
  20. 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

11 authors at 1 institution in 1 country.

Heather L CaslinVirginia Commonwealth University Life Sciences, Virginia Commonwealth University, Richmond, VA 23284.
Daniel AbebayehuDepartment of Biology, Virginia Commonwealth University, Richmond, VA 23284.ORCID 0000-0002-6837-3028
Amina Abdul QayumDepartment of Biology, Virginia Commonwealth University, Richmond, VA 23284.
Tamara T HaqueDepartment of Biology, Virginia Commonwealth University, Richmond, VA 23284.
Marcela T TaruselliDepartment of Biology, Virginia Commonwealth University, Richmond, VA 23284.
Patrick A PaezDepartment of Biology, Virginia Commonwealth University, Richmond, VA 23284.ORCID 0000-0003-0746-7204
Neha PondicherryDepartment of Biology, Virginia Commonwealth University, Richmond, VA 23284.
Brian O BarnsteinDepartment of Biology, Virginia Commonwealth University, Richmond, VA 23284.
L Alexis HoeferlinDepartment of Biochemistry, Virginia Commonwealth University, Richmond, VA 23298.ORCID 0000-0001-7569-8712
Charles E ChalfantDepartment of Biochemistry, Virginia Commonwealth University, Richmond, VA 23298.ORCID 0000-0002-5844-5235
John J RyanDepartment of Biology, Virginia Commonwealth University, Richmond, VA 23284; jjryan@vcu.edu.
Virginia Commonwealth University · US

Funding

The utilization of photonics technology to rapidly detect bioactive lipids associated with preeclampsia developmentU01HD087198 · NICHD · VIRGINIA COMMONWEALTH UNIVERSITY · PI CHALFANT, CHARLES E., WALSH, SCOTT W · 2015 to 2015
$4.2M
The functional role of the cPLA2alpha/C1P interaction in sepsis resolutionR01HL125353 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI BROWN, RHODERICK E, CHALFANT, CHARLES E. · 2014 to 2018
$4.0M
IL-10 Regulates Mast Cell Function and SurvivalR01AI059638 · NIAID · VIRGINIA COMMONWEALTH UNIVERSITY · PI RYAN, JOHN J · 2007 to 2017
$3.8M
GGT Targeting Suppresses Mast Cell Activation by IgE and IL-33R01AI138495 · NIAID · VIRGINIA COMMONWEALTH UNIVERSITY · PI RYAN, JOHN J · 2018 to 2022
$2.2M
Control of IgG-mediated Inflammation by Fyn and Lyn KinasesR01AI101153 · NIAID · VIRGINIA COMMONWEALTH UNIVERSITY · PI RYAN, JOHN J · 2013 to 2017
$2.0M
SSRIs Inhibit IgE-mediated Mast Cell FunctionR21AI138494 · NIAID · VIRGINIA COMMONWEALTH UNIVERSITY · PI RYAN, JOHN J · 2019 to 2020
$403k
BLRD VA I01 BX001792NHLBI NIH HHS R01 HL125353NIAID NIH HHS R01 AI059638NIAID NIH HHS R01 AI101153NIAID NIH HHS R01 AI138495NIAID NIH HHS R21 AI138494NICHD NIH HHS U01 HD087198
6 · The paper itself

Abstract

Sepsis has a well-studied inflammatory phase, with a less-understood secondary immunosuppressive phase. Elevated blood lactate and slow lactate clearance are associated with mortality; however, regulatory roles are unknown. We hypothesized that lactic acid (LA) contributes to the late phase and is not solely a consequence of bacterial infection. No studies have examined LA effects in sepsis models in vivo or a mechanism by which it suppresses LPS-induced activation in vitro. Because mast cells can be activated systemically and contribute to sepsis, we examined LA effects on the mast cell response to LPS. LA significantly suppressed LPS-induced cytokine production and NF-κB transcriptional activity in mouse bone marrow-derived mast cells and cytokine production in peritoneal mast cells. Suppression was MCT-1 dependent and reproducible with sodium lactate or formic acid. Further, LA significantly suppressed cytokine induction following LPS-induced endotoxemia in mice. Because glycolysis is linked to inflammation and LA is a byproduct of this process, we examined changes in glucose metabolism. LA treatment reduced glucose uptake and lactate export during LPS stimulation. LA effects were mimicked by glycolytic inhibitors and reversed by increasing ATP availability. These results indicate that glycolytic suppression and ATP production are necessary and sufficient for LA effects. Our work suggests that enhancing glycolysis and ATP production could improve immune function, counteracting LA suppressive effects in the immunosuppressive phase of sepsis.

Indexed as

Adenosine TriphosphateAnimalsCytokinesEndotoxemiaGlycolysisInflammationLactic AcidLipopolysaccharidesMast CellsMiceMice, Inbred C57BLSepsisSignal TransductionAdenosine TriphosphateCytokinesLactic AcidLipopolysaccharides

Identifiers

PMID31160535
PMCPMC6734564
OpenAlexW2948677864

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.