Evidence map›Paper›PMID 33584659›Full record

ArticleFrontiers in immunology2020

Myosin Light Chain 9/12 Regulates the Pathogenesis of Inflammatory Bowel Disease.

Masaya Yokoyama, Motoko Y Kimura, Toshihiro Ito, Koji Hayashizaki, Yukihiro Endo, Yangsong Wang, Ryoji Yagi, Tomoo Nakagawa, Naoya Kato, Hisahiro Matsubara and 1 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Differentiation of Cytotoxic CD8Cancer science · 2025
    Review
  5. T cells in cardiac health and disease.The Journal of clinical investigation · 2025
    Review
  6. Article
  7. Article
  8. Alleviation of LPS-induced Endothelial Injury due to GHRH Antagonist Treatment.International journal of peptide research and therapeutics · 2024
    Article
  9. Article
  10. Differential Protein Expression ofPathogens (Basel, Switzerland) · 2023
    Article
  11. Article
  12. Article
  13. 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

11 authors.

Masaya YokoyamaDepartment of Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Motoko Y KimuraDepartment of Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Toshihiro ItoDepartment of Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Koji HayashizakiDepartment of Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Yukihiro EndoDepartment of Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Yangsong WangDepartment of Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Ryoji YagiDepartment of Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Tomoo NakagawaDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Naoya KatoDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Hisahiro MatsubaraDepartment of Frontier Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.
Toshinori NakayamaDepartment of Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The numbers of patients with inflammatory bowel disease (IBD), such as ulcerative colitis (UC) and Crohn's disease (CD), have been increasing over time, worldwide; however, the pathogenesis of IBD is multifactorial and has not been fully understood. Myosin light chain 9 and 12a and 12b (Myl9/12) are known as ligands of the CD69 molecule. They create "Myl9 nets" that are often detected in inflamed site, which play a crucial role in regulating the recruitment and retention of CD69-expressing effector cells in inflamed tissues. We demonstrated the strong expression of Myl9/12 in the inflamed gut of IBD patients and mice with DSS-induced colitis. The administration of anti-Myl9/12 Ab to mice with DSS-induced colitis ameliorated the inflammation and prolonged their survival. The plasma Myl9 levels in the patients with active UC and CD were significantly higher than those in patients with disease remission, and may depict the disease severity of IBD patients, especially those with UC. Thus, our results indicate that Myl9/12 are involved in the pathogenesis of IBD, and are likely to be a new therapeutic target for patients suffering from IBD.

Indexed as

Disease SusceptibilityAdultAgedAnimalsAntibodies, MonoclonalBiomarkersCase-Control StudiesDiagnosis, DifferentialDisease Models, AnimalEnzyme-Linked Immunosorbent AssayFemaleGene ExpressionHumansImmunohistochemistryInflammatory Bowel DiseasesIntestinal MucosaAntibodies, MonoclonalBiomarkersMYL9 protein, humanMyosin Light ChainsCD69Crohn’s diseaseMyl9plasma biomarkerulcerative colitis

Identifiers

PMID33584659
PMCPMC7878395

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.