Evidence map›Paper›PMID 20299601›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2010

Exploring the interplay of barrier function and leukocyte recruitment in intestinal inflammation by targeting fucosyltransferase VII and trefoil factor 3.

P L Beck, E Ihara, S A Hirota, J A MacDonald, D Meng, N N Nanthakumar, D K Podolsky, R J Xavier

Abstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. International journal of molecular sciences · 2021
    Article
  5. Renin-angiotensin system promotes colonic inflammation by inducing TAmerican journal of physiology. Gastrointestinal and liver physiology · 2019
    Article
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  15. Targeting Hypoxia to Augment Mucosal Barrier Function.Journal of epithelial biology & pharmacology · 2012
    Article
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

8 authors at 3 institutions in 2 countries.

P L BeckGastrointestinal Research Group, University of Calgary, Calgary, Alberta, Canada T2N 4N1. plbeck@ucalgary.ca
E Ihara
S A Hirota
J A MacDonald
D Meng
N N Nanthakumar
D K Podolsky
R J Xavier
University of Calgary · CAMassachusetts General Hospital · USThe University of Texas Southwestern Medical Center · US

Funding

Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG · 1991 to 2026
$35.3M
ROLE OF DIETARY CONSTITUENTS ON GENE EXPRESSION IN INTESTINAL EPITHELIUMP30DK040561 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI CHRISTOPHER P DUGGAN · 1994 to 2026
$31.6M
Toll-like Receptors and the Intestinal EpitheliumR01DK060049 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI XAVIER, RAMNIK J · 2002 to 2011
$3.5M
EFFECT OF COLOSTRUM ON GUT MATURATION AND HOST DEFENSER37HD012437 · NICHD · MASSACHUSETTS GENERAL HOSPITAL · PI WALKER, W ALLAN · 1997 to 2006
$2.2M
Maturation of intestinal innate immunity and NECR01HD059126 · NICHD · MASSACHUSETTS GENERAL HOSPITAL · PI WALKER, W ALLAN · 2009 to 2013
$2.2M
EFFECT OF COLOSTRUM ON GUT MATURATION AND HOST DEFENSER01HD012437 · NICHD · MASSACHUSETTS GENERAL HOSPITAL · PI WALKER, W ALLAN · 1989 to 2013
$2.0M
Ontogeny of the intestinal mucosal barrier and NECR01DK070260 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI WALKER, W ALLAN · 2005 to 2009
$1.8M
Systems Biology of Crohn's DiseaseR01DK083756 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI DALY, MARK JOSEPH, XAVIER, RAMNIK J · 2008 to 2011
$1.5M
THE EFFECT OF COLOSTRUM ON GUT MATURATION AND HOST DEFENR22HD012437 · NICHD · MASSACHUSETTS GENERAL HOSPITAL · PI WALKER, W ALLAN · 1985 to 1991
–
CIHRNICHD NIH HHS HD059126NICHD NIH HHS HD12437NICHD NIH HHS R01 HD012437NICHD NIH HHS R01 HD059126NICHD NIH HHS R37 HD012437NIDDK NIH HHS DK043351NIDDK NIH HHS DK70260NIDDK NIH HHS DK83756NIDDK NIH HHS P30 DK040561NIDDK NIH HHS R01 DK060049NIDDK NIH HHS R01 DK070260
6 · The paper itself

Abstract

Intestinal mucosal integrity is dependent on epithelial function and a regulated immune response to injury. Fucosyltransferase VII (Fuc-TVII) is an essential enzyme required for the expression of the functional ligand for E- and P-selectin. Trefoil factor 3 (TFF3) is involved in both protecting the intestinal epithelium against injury as well as aiding in wound repair following injury. The aim of the present study was to assess the interplay between barrier function and leukocyte recruitment in intestinal inflammation. More specifically, we aimed to examine how targeted disruption of Fuc-TVII either in wild-type or TFF3(-/-) mice would alter their susceptibility to colonic injury. TFF3 and Fuc-TVII double-knockout mice (TFF3/Fuc-TVII(-/-) mice) were generated by mating TFF3(-/-) and Fuc-TVII(-/-) mice. Colitis was induced by administration of dextran sodium sulfate (DSS) (2.5% wt/vol) in the drinking water. Changes in baseline body weight, diarrhea, and fecal blood were assessed daily. Upon euthanasia, extents of colonic inflammation were assessed macroscopically, microscopically, and through quantification of myeloperoxidase (MPO) activity. Colonic lymphocyte subpopulations were assessed at 6 days after administration of DSS by flow cytometry and immunohistochemistry. No baseline intestinal inflammation was found in TFF3/Fuc-TVII(-/-), TFF3(-/-), Fuc-TVII(-/-), or wild-type mice. Loss of Fuc-TVII resulted in a reduction in disease severity whereas TFF3(-/-) mice were markedly more susceptible to DSS-induced colitis. Remarkably, the loss of Fuc-TVII in TFF3(-/-) mice markedly decreased the severity of DSS-induced colitis as evidenced by reduced weight loss, diarrhea, decreased colonic MPO levels and improved survival. Furthermore, the loss of TFF3 resulted in increased severity of spontaneous colitis in IL-2/beta-microglobulin-deficient mice. These studies highlight the importance of the interplay between factors involved in the innate immune response, mucosal barrier function, and genes involved in regulating leukocyte recruitment and other aspects of the immune response.

Indexed as

Chemotaxis, LeukocyteImmunity, InnateAnimalsbeta 2-MicroglobulinColitisDextran SulfateDiarrheaDisease Models, AnimalFucosyltransferasesInterleukin-2Intestinal MucosaLeukocytesMelenaMiceMice, Inbred C57BLMice, Knockoutbeta 2-MicroglobulinDextran SulfateFucosyltransferasesfucosyltransferase VII, mouseInterleukin-2MucinsPeroxidaseTff3 protein, mouseTrefoil Factor-3

Identifiers

PMID20299601
PMCPMC2904110
OpenAlexW2151511969

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.