Evidence map›Paper›PMID 12235077›Full record

ArticleGut2002

Upregulation of matrix metalloproteinases in a model of T cell mediated tissue injury in the gut: analysis by gene array and in situ hybridisation.

M T Salmela, T T MacDonald, D Black, B Irvine, T Zhuma, U Saarialho-Kere, S L F Pender

Open access · bronzeAbstract read
In one paragraph

Article in Gut, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

40 citing papers in PubMed, 109 citations in OpenAlex.

  1. Review
  2. Proteases in intestinal health and disease.Nature reviews. Gastroenterology & hepatology · 2026
    Review
  3. Article
  4. Article
  5. Selected Cytokines and Metalloproteinases in Inflammatory Bowel Disease.International journal of molecular sciences · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Metalloproteinases in Inflammatory Bowel Diseases.Journal of inflammation research · 2021
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. The Role of Gelatinases in Campylobacter Jejuni Infection of Gnotobiotic Mice.European journal of microbiology & immunology · 2015
    Article
  17. Article
  18. Article
  19. Article
  20. 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

7 authors at 3 institutions in 2 countries.

M T SalmelaDepartment of Dermatology, Helsinki University Central Hospital, Helsinki, Finland.
T T MacDonald
D Black
B Irvine
T Zhuma
U Saarialho-Kere
S L F Pender
Pfizer (United Kingdom) · GBHelsinki University Hospital · FIUniversity of Southampton · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimMatrix metalloproteinases (MMPs) have been implicated in tissue remodelling and ulceration in inflammatory bowel disease and coeliac disease. Studies to date have concluded that stromelysin 1 is functionally involved in mucosal degradation. However, there are many other MMPs whose function in the gut is currently unknown. This work had two aims: firstly, to use gene array technology to measure changes in MMP and tissue inhibitor of metalloproteinase (TIMP) expression in a model of T cell mediated injury in the gut, and secondly, to correlate data from gene arrays with that generated by in situ hybridisation.

methodsT cells in explants of human fetal gut were activated with pokeweed mitogen or anti-CD3 plus interleukin 12. Gene array analysis and in situ hybridisation were performed to investigate changes in MMP gene expression.

resultsBoth gene array analysis and in situ hybridisation indicated marked upregulation of stromelysin 2 and macrophage metalloelastase expression in the explants associated with mucosal destruction. The arrays also confirmed our previous observation that interstitial collagenase (MMP-1), stromelysin 1 (MMP-3), and gelatinase B (MMP-9) are upregulated but there was no change in MMP-2, -7, -8, -9, -11, -13, -14-17, or -19. Following T cell activation, transcripts for TIMPs were reduced.

conclusionsThese results show that there is differential upregulation of MMPs during T cell responses in the gut and suggest that further studies on the role of stromelysin 2 and macrophage metalloelastase may show that they have a functional role. In addition, the increase in MMPs and reduction in TIMPs suggest that the protease/antiprotease balance in the mucosa may determine the extent of mucosal degradation.

Indexed as

Up-RegulationCollagenasesHumansIn Situ HybridizationIntestine, SmallMatrix Metalloproteinase 10Matrix Metalloproteinase 12Matrix Metalloproteinase 13Matrix Metalloproteinase 7Matrix MetalloproteinasesMatrix Metalloproteinases, Membrane-AssociatedMetalloendopeptidasesOligonucleotide Array Sequence AnalysisRNATissue Inhibitor of Metalloproteinase-1Tissue Inhibitor of Metalloproteinase-3CollagenasesMatrix Metalloproteinase 10Matrix Metalloproteinase 12Matrix Metalloproteinase 13Matrix Metalloproteinase 7Matrix MetalloproteinasesMatrix Metalloproteinases, Membrane-AssociatedMetalloendopeptidasesMMP12 protein, humanMMP13 protein, humanRNATissue Inhibitor of Metalloproteinase-1Tissue Inhibitor of Metalloproteinase-3Tissue Inhibitor of Metalloproteinases

Identifiers

PMID12235077
PMCPMC1773375
OpenAlexW2101384136

What OpenQuestion holds

Textmetadata
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Registered trials

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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.