Evidence map›Paper›PMID 33594081›Full record

ArticleNature communications2021

Pancreatic glycoprotein 2 is a first line of defense for mucosal protection in intestinal inflammation.

Yosuke Kurashima, Takaaki Kigoshi, Sayuri Murasaki, Fujimi Arai, Kaoru Shimada, Natsumi Seki, Yun-Gi Kim, Koji Hase, Hiroshi Ohno, Kazuya Kawano and 12 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
3.8field-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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
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  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Update on Autoimmune Pancreatitis and IgG4-Related Disease.United European gastroenterology journal · 2025
    Review
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  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. The oral-gut axis: a missing piece in the IBD puzzle.Inflammation and regeneration · 2023
    Review
  20. Polysaccharide fromNutrients · 2023
    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

22 authors at 10 institutions in 2 countries.

Yosuke Kurashima *Department of Mucosal Immunology, The University of Tokyo Distinguished Professor Unit, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan. yosukek@chiba-u.jp.
Takaaki Kigoshi *Department of Mucosal Immunology, The University of Tokyo Distinguished Professor Unit, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.ORCID http://orcid.org/0000-0002-6984-475X
Sayuri MurasakiDepartment of Mucosal Immunology, The University of Tokyo Distinguished Professor Unit, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Fujimi AraiDepartment of Mucosal Immunology, The University of Tokyo Distinguished Professor Unit, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Kaoru ShimadaDepartment of Mucosal Immunology, The University of Tokyo Distinguished Professor Unit, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Natsumi SekiDivision of Biochemistry, Graduate School of Pharmacological Science, Keio University, Tokyo, Japan.
Yun-Gi KimResearch Center for Drug Discovery, Faculty of Pharmacy, Keio University, Tokyo, Japan.
Koji HaseInternational Research and Development Center for Mucosal Vaccines, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.ORCID http://orcid.org/0000-0001-9550-2334
Hiroshi OhnoLaboratory for Intestinal Ecosystem, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan.ORCID http://orcid.org/0000-0001-8776-9661
Kazuya KawanoLaboratory for Intestinal Ecosystem, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan.
Hiroshi AshidaDepartment of Bacterial Infection and Host Response, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
Toshihiko SuzukiDepartment of Bacterial Infection and Host Response, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
Masako MorimotoDepartment of Innovative Medicine, Graduate School of Medicine, Chiba University, Chiba, Japan.
Yukari SaitoDepartment of Innovative Medicine, Graduate School of Medicine, Chiba University, Chiba, Japan.
Ai SasouDepartment of Mucosal Immunology, The University of Tokyo Distinguished Professor Unit, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Yuki GodaDepartment of Mucosal Immunology, The University of Tokyo Distinguished Professor Unit, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Yoshikazu YukiDepartment of Mucosal Immunology, The University of Tokyo Distinguished Professor Unit, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Yutaka InagakiCenter for Matrix Biology and Medicine, Graduate School of Medicine, Tokai University, Kanagawa, Japan.ORCID http://orcid.org/0000-0001-6640-7688
Hideki IijimaDepartment of Gastroenterology and Hepatology, Graduate School of Medicine, Osaka University, Osaka, Japan.
Wataru SudaLaboratory for Microbiome Sciences, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan.
Masahira HattoriLaboratory for Microbiome Sciences, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan.
Hiroshi KiyonoDepartment of Mucosal Immunology, The University of Tokyo Distinguished Professor Unit, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan. hkiyono@health.ucsd.edu.ORCID http://orcid.org/0000-0001-7307-4658
The University of Tokyo · JPChiba University · JPKeio University · JPRIKEN Center for Integrative Medical Sciences · JPTokyo Medical and Dental University · JPKanagawa Industrial Technology Center · JPThe University of Osaka · JPTohoku University · JPTokai University · JPWaseda University · JP

Funding

San Diego Digestive Diseases Research CenterP30DK120515 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Bernd G. Schnabl · 2019 to 2026
$10.8M
NIDDK NIH HHS P30 DK120515
6 · The paper itself

Abstract

Increases in adhesive and invasive commensal bacteria, such as Escherichia coli, and subsequent disruption of the epithelial barrier is implicated in the pathogenesis of inflammatory bowel disease (IBD). However, the protective systems against such barrier disruption are not fully understood. Here, we show that secretion of luminal glycoprotein 2 (GP2) from pancreatic acinar cells is induced in a TNF-dependent manner in mice with chemically induced colitis. Fecal GP2 concentration is also increased in Crohn's diease patients. Furthermore, pancreas-specific GP2-deficient colitis mice have more severe intestinal inflammation and a larger mucosal E. coli population than do intact mice, indicating that digestive-tract GP2 binds commensal E. coli, preventing epithelial attachment and penetration. Thus, the pancreas-intestinal barrier axis and pancreatic GP2 are important as a first line of defense against adhesive and invasive commensal bacteria during intestinal inflammation.

Indexed as

Acinar CellsAnimalsColitisCytokinesDextran SulfateEscherichia coliFecesGreen Fluorescent ProteinsHumansImmunoglobulin AInflammationIntestinal MucosaMembrane GlycoproteinsMiceMice, Inbred C57BLPancreasCytokinesDextran Sulfateglycoprotein-2, pancreasGreen Fluorescent ProteinsImmunoglobulin AMembrane GlycoproteinsRecombinant Proteinstranscription factor PTF1Transcription Factors

Identifiers

PMID33594081
PMCPMC7887276
OpenAlexW3129786277

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.