Evidence map›Paper›PMID 24268632›Full record

ArticleVeterinary immunology and immunopathology2014

Epigenetic contribution to individual variation in response to lipopolysaccharide in bovine dermal fibroblasts.

Benjamin B Green, David E Kerr

Abstract read
In one paragraph

Article in Veterinary immunology and immunopathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Differential expression of serum amyloid A1 and A3 in bovine epithelia.The Journal of veterinary medical science · 2020
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Epigenetics and transgenerational inheritance in domesticated farm animals.Journal of animal science and biotechnology · 2014
    Review
  18. Bovine mastitis: frontiers in immunogenetics.Frontiers in immunology · 2014
    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

2 authors at 1 institution in 1 country.

Benjamin B GreenTerrill Hall, University of Vermont, 570 Main Street, Burlington 05405, United States.
David E KerrTerrill Hall, University of Vermont, 570 Main Street, Burlington 05405, United States. Electronic address: david.kerr@uvm.edu.
University of Vermont · US

Funding

VOLATILE SIGNALING IN PHARBITIS NILP20RR016462 · NCRR · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI KIRSHENBAUM, ARI PHILLIP · 2001 to 2011
$31.1M
NCRR NIH HHS P20 RR016462NCRR NIH HHS P20 RR16462
6 · The paper itself

Abstract

The innate immune signaling pathway plays a crucial role in the recognition and early response to pathogens associated with disease. Genetic analysis has been unable to completely account for individual variability in the strength of the innate immune response. The aim of this study was to determine the role of the epigenetic markers (DNA methylation or histone acetylation) in controlling bovine gene expression in relation to the response to lipopolysaccharide (LPS). To determine the impact epigenetics may have in controlling innate immunity, dermal fibroblasts from fifteen dairy heifers having previously displayed a differential response to LPS were exposed to 5-aza-2'-deoxycytidine (AZA) and trichostatin A (TSA); de-methylating and hyper-acetylating agents, respectively. The AZA-TSA exposure resulted in a loss of variability between individuals' response to LPS as measured by fibroblast IL-8 protein production. Transcriptomic analysis by microarray was used to elucidate the role of epigenetics in innate immune signaling at 2, 4, and 8h post-LPS exposure. A subset of genes displayed altered expression due to AZA-TSA alone, suggesting an epigenetic regulatory element modifying expression under normal conditions. Treatment with AZA-TSA also led to increased expression of IL-8 (7.0-fold), IL-6 (2.5-fold), TNF-α (1.6-fold), and serum amyloid A 3 (SAA3) (11.3-fold) among other genes compared to control cultures for at least one of the measured times following LPS exposure. These data support the conclusion that epigenetic regulation significantly alters LPS-induced responses and constitutive cytokine gene expression.

Indexed as

AcetylationAnimalsAzacitidineCattleDecitabineDNA MethylationEpigenesis, GeneticFemaleFibroblastsGene Expression RegulationHydroxamic AcidsImmunity, InnateInterleukinsLipopolysaccharidesOligonucleotide Array Sequence AnalysisReal-Time Polymerase Chain ReactionAzacitidineDecitabineHydroxamic AcidsInterleukinsLipopolysaccharidesRNASerum Amyloid A Proteintrichostatin ATumor Necrosis Factor-alphaAcetylationInnate immunityMethylationTLR4

Identifiers

PMID24268632
PMCPMC4228796
OpenAlexW1977577669

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.