Evidence map›Paper›PMID 22131549›Full record

ArticleThe Journal of nutrition2012

Th17 cell accumulation is decreased during chronic experimental colitis by (n-3) PUFA in Fat-1 mice.

Jennifer M Monk, Qian Jia, Evelyn Callaway, Brad Weeks, Robert C Alaniz, David N McMurray, Robert S Chapkin

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of nutrition, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.5field-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

46 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
  2. Review
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  5. Age-specific Metabolomic profiles in children with food allergy.Clinical immunology (Orlando, Fla.) · 2024
    Article
  6. Article
  7. Review
  8. Article
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  10. Article
  11. Review
  12. EndogenousInternational journal of molecular sciences · 2019
    Article
  13. Review
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  15. Review
  16. Article
  17. Review
  18. Review
  19. Regulation of T cell signalling by membrane lipids.Nature reviews. Immunology · 2016
    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

7 authors at 2 institutions in 1 country.

Jennifer M MonkProgram in Integrative Nutrition and Complex Diseases, Texas A&M University System Health Science Center, Texas A&M University, College Station, TX, USA.
Qian Jia
Evelyn Callaway
Brad Weeks
Robert C Alaniz
David N McMurray
Robert S Chapkin
Texas A&M University · USTexas A&M University System · US

Funding

Colonic Cytokinetics and Cell Signaling: Dietary EffectsR01CA059034 · NCI · TEXAS A&M UNIVERSITY SYSTEM · PI CHAPKIN, ROBERT STEPHEN · 1995 to 2012
$3.6M
N-3 Fatty Acids Alter T Cell Activation and SignalingR01DK071707 · NIDDK · TEXAS A&M UNIVERSITY · PI CHAPKIN, ROBERT STEPHEN · 2007 to 2011
$1.5M
NIDDK NIH HHS DK071707NIDDK NIH HHS R01 DK071707
6 · The paper itself

Abstract

During colon inflammation, Th17 cells and immunosuppressive regulatory T cells (Treg) are thought to play promotive and preventative roles, respectively. Dietary (n-3) PUFA favorably modulate intestinal inflammation in part by downregulating T-cell activation and functionality. We used the Fat-1 mouse, a genetic model that synthesizes long-chain (n-3) PUFA de novo, to test the hypothesis that (n-3) PUFA protect against colonic inflammation by modulating the polarization of Treg and Th17 cells during colitis. Male and female wild-type (WT) and Fat-1 mice were administered dextran sodium sulfate (DSS) in the drinking water (2.5%) to induce acute (5 d DSS) or chronic (3 cycles DSS) colitis and the percentage of Treg and Th17 cells residing locally [colonic lamina propria (cLP)] and systemically (spleen) was determined by flow cytometry. The percentage of Treg in either tissue site was unaffected by genotype (P > 0.05); however, during chronic colitis, the percentage of Th17 cells residing in both the spleen and cLP was lower in Fat-1 mice compared to WT mice (P < 0.05). Colonic mucosal mRNA expression of critical Th17 cell cytokines and chemokine receptors (IL-17F, IL-21, and CCR6) were lower, whereas expression of the Th17 cell suppressive cytokine, IL-27, was greater in Fat-1 mice compared to WT mice during chronic colitis (P < 0.05). Moreover, colon histological scores were improved in Fat-1 mice (P < 0.05). Collectively, these results demonstrate for the first time, to our knowledge, that (n-3) PUFA can modulate the colonic mucosal microenvironment to suppress Th17 cell accumulation and inflammatory damage following the induction of chronic colitis.

Indexed as

AnimalsChronic DiseaseColitisCytokinesFatty Acids, Omega-3FemaleFlow CytometryMaleMiceMice, Mutant StrainsTh17 CellsCytokinesFatty Acids, Omega-3

Identifiers

PMID22131549
PMCPMC3237233
OpenAlexW2116325113

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.