Evidence map›Paper›PMID 16299040›Full record

ArticleGut2006

Induction of a fibrogenic response in mouse colon by overexpression of monocyte chemoattractant protein 1.

Y Motomura, W I Khan, R T El-Sharkawy, M Verma-Gandhu, E F Verdu, J Gauldie, S M Collins

Open access · bronzeAbstract read
In one paragraph

Article in Gut, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.2field-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

20 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  6. Article
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  8. Article
  9. Review
  10. Article
  11. Animal models of intestinal fibrosis: new tools for the understanding of pathogenesis and therapy of human disease.American journal of physiology. Gastrointestinal and liver physiology · 2012
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Substance P modulates colitis-associated fibrosis.The American journal of pathology · 2010
    Article
  18. Intestinal fibrosis in IBD--a dynamic, multifactorial process.Nature reviews. Gastroenterology & hepatology · 2009
    Review
  19. Article
  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 1 institution in 1 country.

Y MotomuraIntestinal Diseases Research programme, McMaster University, Hamilton, Ontario, Canada. yasumm@gmail.com
W I Khan
R T El-Sharkawy
M Verma-Gandhu
E F Verdu
J Gauldie
S M Collins
McMaster University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsMonocyte chemoattractant protein 1 (MCP-1) is increased transmurally in inflammatory bowel disease (IBD). Although MCP-1 is considered to play an important role in fibrotic disease in other organs, the role of MCP-1 in gut fibrosis is unknown. We investigated the fibrotic potential of MCP-1 in the gut by overexpressing this chemokine in the mouse colorectal wall.

methodsIntramural gene transfer by direct injection of adenovector into the mouse rectal wall was established. C57BL/6 and Rag2(-/-) (B and T cell deficient) mice received 2.5 x 10(9) plaque forming units of an adenovector encoding murine MCP-1 (AdMCP-1) or control virus (AdDL70) via intramural injection. Mice were killed at various time points and tissues were obtained for histopathological and biochemical analysis.

resultsAdMCP-1 significantly increased collagen production in the colorectum and this was associated with significant elevation of transforming growth factor beta (TGF-beta) and tissue inhibitor of metalloproteinase (TIMP-1) protein. Transmural collagen deposition was observed after AdMCP-1 administration, and was accompanied by CD3+ T cells, F4/80+ macrophages, and vimentin+ cell infiltrates. Collagen was differentially distributed, with type I deposited in the muscularis mucosa and muscularis propria and type III in the submucosa and myenteric plexus. AdMCP-1 failed to induce collagen overproduction in immunodeficient Rag2(-/-) mice.

conclusionThese findings suggest that MCP-1 can induce fibrosis in the gut and that this process involves interaction between T cells and vimentin positive fibroblasts/myofibroblasts, as well as the subsequent upregulation of TGF-beta and TIMP-1 production. This model provides a basis for considering MCP-1 in the pathogenesis of strictures in IBD.

Indexed as

AdenoviridaeAnimalsChemokine CCL2Collagen Type ICollagen Type IIIColonEnzyme-Linked Immunosorbent AssayFibrosisGenetic VectorsHistocytochemistryImmunohistochemistryLymphocytesMaleMatrix Metalloproteinase 3MiceMice, Inbred C57BLChemokine CCL2Collagen Type ICollagen Type IIIMatrix Metalloproteinase 3Tissue Inhibitor of Metalloproteinase-1Transforming Growth Factor beta

Identifiers

PMID16299040
PMCPMC1856110
OpenAlexW2119493317

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.