Evidence map›Paper›PMID 21415414›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2011

Occludin regulates macromolecule flux across the intestinal epithelial tight junction barrier.

Rana Al-Sadi, Khaldun Khatib, Shuhong Guo, Dongmei Ye, Moustafa Youssef, Thomas Ma

Abstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 202 papers.

0numbers the graph read from it
0cells of the map it votes in
202citing papers in PubMed
13.9field-weighted citation impact, top 1% 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

202 citing papers in PubMed, 403 citations in OpenAlex.

  1. Article
  2. Article
  3. Metabolite mimicry identifies butyrate analogs with select protective functions in the intestinal mucosa.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  17. Immunomodulation ofFoods (Basel, Switzerland) · 2025
    Article
  18. Article
  19. Article
  20. Article

142 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 1 country.

Rana Al-SadiDepartment of Internal Medicine, University of New Mexico, Albuquerque, NM 87131-0001, USA.
Khaldun Khatib
Shuhong Guo
Dongmei Ye
Moustafa Youssef
Thomas Ma
University of New Mexico · US

Funding

TNF-alpha Regulation of Intestinal Paracellular TransportR01DK064165 · NIDDK · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI MA, THOMAS Y · 2003 to 2018
$5.2M
Interleukin-1 Beta Modulation of Intestinal Tight Junction BarrierR01DK081429 · NIDDK · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI MA, THOMAS Y · 2009 to 2012
$1.4M
NIDDK NIH HHS R0 1-DK-64165NIDDK NIH HHS R0 1-DK-81429
6 · The paper itself

Abstract

Defective intestinal epithelial tight junction (TJ) barrier has been shown to be an important pathogenic factor contributing to the development of intestinal inflammation. The expression of occludin is markedly decreased in intestinal permeability disorders, including in Crohn's disease, ulcerative colitis, and celiac disease, suggesting that the decrease in occludin expression may play a role in the increase in intestinal permeability. The purpose of this study was to delineate the involvement of occludin in intestinal epithelial TJ barrier by selective knock down of occludin in in vitro (filter-grown Caco-2 monolayers) and in vivo (recycling perfusion of mouse intestine) intestinal epithelial models. Our results indicated that occludin small-interfering RNA (siRNA) transfection causes an increase in transepithelial flux of various-sized probes, including urea, mannitol, inulin, and dextran, across the Caco-2 monolayers, without affecting the transepithelial resistance. The increase in relative flux rate was progressively greater for larger-sized probes, indicating that occludin depletion has the greatest effect on the flux of large macromolecules. siRNA-induced knock down of occludin in mouse intestine in vivo also caused an increase in intestinal permeability to dextran but did not affect intestinal tissue transepithelial resistance. In conclusion, these results show for the first time that occludin depletion in intestinal epithelial cells in vitro and in vivo leads to a selective or preferential increase in macromolecule flux, suggesting that occludin plays a crucial role in the maintenance of TJ barrier through the large-channel TJ pathway, the pathway responsible for the macromolecule flux.

Indexed as

AnimalsBiological TransportCaco-2 CellsDown-RegulationElectric ImpedanceHumansIntestinal MucosaMaleMembrane ProteinsMiceMice, Inbred C57BLMolecular ProbesMolecular WeightOccludinParticle SizePermeabilityMembrane ProteinsMolecular ProbesOccludinOCLN protein, humanOcln protein, mouse

Identifiers

PMID21415414
PMCPMC3119114
OpenAlexW2166338423

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.