Evidence map›Paper›PMID 11559650›Full record

ArticleGut2001

MIP-2 secreted by epithelial cells increases neutrophil and lymphocyte recruitment in the mouse intestine.

Y Ohtsuka, J Lee, D S Stamm, I R Sanderson

Open access · bronzeAbstract read
In one paragraph

Article in Gut, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

68 citing papers in PubMed, 152 citations in OpenAlex.

  1. Article
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  6. Mediators of inflammation · 2025
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  9. The Antioxidant Properties ofAntioxidants (Basel, Switzerland) · 2023
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  18. A New Understanding of the Role of IL-1 in Age-Related Intervertebral Disc Degeneration in a Murine Model.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2019
    Article
  19. Article
  20. Article

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

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

4 authors at 1 institution in 2 countries.

Y OhtsukaDepartment of Adult and Paediatric Gastroenterology, St Bartholomew's and the Royal London School of Medicine and Dentistry, London, UK.
J Lee
D S Stamm
I R Sanderson
St Bartholomew's Hospital · GB

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
BUTYRATE REGULATION OF IMMUNE FUNCTIONS OF ENTEROCYTESR01AI043472 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI WALKER, W ALLAN · 1998 to 2001
$291k
CLASS II MHC AND COSTIMULATORY MOLECULES IN ENTEROCYTESR29DK047753 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI SANDERSON, IAN R · 1995 to 1999
–
NIAID NIH HHS AI43472NIDDK NIH HHS DK40561NIDDK NIH HHS DK43351NIDDK NIH HHS DK47753
6 · The paper itself

Abstract

backgroundInvasion of the intestinal mucosa by leucocytes is a characteristic of intestinal inflammation but the role of the epithelium in orchestrating this recruitment has not been examined in vivo. Cultured intestinal epithelial cells secrete a wide variety of chemokines, often in response to agents present in the intestinal lumen. Macrophage inflammatory protein 2 (MIP-2) is a chemokine that attracts neutrophils, and its secretion from intestinal epithelial cells is enhanced by inflammatory stimuli such as interleukin 1beta. We hypothesised that the production of MIP-2 by epithelial cells would increase leucocyte migration into the intestine.

aimTo study the effects of a chemokine secreted from intestinal epithelial cells in vivo.

methodsMIP-2 was expressed in the mouse intestinal epithelium using an epithelial cell specific promoter from the gene encoding the intestinal fatty acid binding protein. The intestines of these transgenic mice were then analysed.

resultsEpithelial cells from transgenic mice expressed MIP-2 but wild-type mice did not. Neutrophil recruitment, examined by myeloperoxidase (MPO) staining and total MPO activity per unit weight of intestine, was significantly increased in transgenic mice in both the small intestine and proximal colon, and this was blocked by anti-MIP-2 antibody treatment. Both intraepithelial and lamina propria lymphocytes were also increased in transgenic mice. They showed chemotactic activity to MIP-2 in the Boyden chambers and expressed MIP-2 receptor (CXCR-2) mRNA confirmed by reverse transcription-polymerase chain reaction.

conclusionThese experiments are the first to show a functional role for epithelial chemokines in vivo and reveal an unexpected role for the neutrophil chemokine MIP-2 in controlling mucosal lymphocyte migration.

Indexed as

AnimalsChemokine CXCL2Chemokines, CXCChemotaxis, LeukocyteEpitheliumImmunity, CellularIntercellular Signaling Peptides and ProteinsIntestinal MucosaLymphocytesMiceMice, TransgenicMonokinesNeutrophil InfiltrationPeroxidaseReceptors, ChemokineReverse Transcriptase Polymerase Chain ReactionChemokine CXCL2Chemokines, CXCCXCL2 protein, humanIntercellular Signaling Peptides and ProteinsMonokinesPeroxidaseReceptors, ChemokineRNA, Messenger

Identifiers

PMID11559650
PMCPMC1728474
OpenAlexW2156201144

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.