Evidence map›Paper›PMID 24169862›Full record

ArticleCell and tissue research2014

Disrupted tight junctions in the small intestine of cystic fibrosis mice.

Robert C De Lisle

Open access · greenAbstract read
In one paragraph

Article in Cell and tissue research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

27 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. The function of chloride channels in digestive system disease (Review).International journal of molecular medicine · 2025
    Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. CFTR, Cell Junctions and the Cytoskeleton.International journal of molecular sciences · 2022
    Review
  10. Review
  11. Synergy in Cystic Fibrosis Therapies: Targeting SLC26A9.International journal of molecular sciences · 2021
    Article
  12. Review
  13. Article
  14. Review
  15. Cystic Fibrosis, CFTR, and Colorectal Cancer.International journal of molecular sciences · 2020
    Review
  16. Nutrients · 2020
    Article
  17. Article
  18. Role of ion channels in gastrointestinal cancer.World journal of gastroenterology · 2019
    Review
  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

1 author at 1 institution in 1 country.

Robert C De LisleAnatomy & Cell Biology, MS 3038, University of Kansas School of Medicine, 3901 Rainbow Blvd., Kansas City, KS, 66160, USA, rdelisle@kumc.edu.
University of Kansas · US

Funding

Impaired intestinal barrier function and airway inflammation in cystic fibrosisR21AI083479 · NIAID · UNIVERSITY OF KANSAS MEDICAL CENTER · PI DE LISLE, ROBERT C · 2009 to 2010
$373k
NIAID NIH HHS AI 083479NIAID NIH HHS R21 AI083479
6 · The paper itself

Abstract

The tight junction (TJ) is the major determinant of paracellular permeability, which in the gut protects the body from entry of harmful substances such as microbial components. In cystic fibrosis (CF), there is increased permeability of the small intestine both in humans and in CF mice. To gain insight into the mechanisms of increased intestinal permeability in CF, I analyze the composition of the TJ in a cystic fibrosis transmembrane conductance regulator (Cftr) knockout mouse model. Significant changes in TJ gene expression in the CF intestine were found for Cldn1, Cldn7, Cldn8 and Pmp22, which were expressed at lower levels and Cldn2 that was expressed at a higher level. Protein levels of claudin-2 were increased in the CF intestine as compared to wild-type, while other TJ proteins were not significantly different. In the villus epithelium of the CF intestine, all TJ components analyzed were mislocalized to the basal cytoplasm and showed varying degrees of loss from the TJ and apico-lateral surfaces. The pore-forming claudin-2 in the CF intestine showed more intense staining but was correctly localized to the TJ, principally in the crypts that are enlarged in CF. The cytokine TNFα, known to affect TJ, was elevated to 160% of wild-type in the CF intestine. In summary, there is a dramatic redistribution of claudin proteins from the TJ/lateral membrane to the basal cytoplasm of the villus epithelium in the CF intestine. These changes in TJ protein localization in CF are likely to be involved in the increased permeability of the CF small intestine to macromolecules and TNFα may be a causative factor.

Indexed as

AnimalsClaudinsCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorCytokinesGene Expression RegulationIntestine, SmallMiceMice, Inbred C57BLMice, KnockoutPermeabilityTight JunctionsClaudinsCystic Fibrosis Transmembrane Conductance RegulatorCytokines

Identifiers

PMID24169862
PMCPMC3904805
OpenAlexW2080081206

What OpenQuestion holds

Textmetadata
LicenceTDM
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.