Evidence map›Paper›PMID 29687905›Full record

ReviewComprehensive Physiology2018

Modulation of Intestinal Paracellular Transport by Bacterial Pathogens.

Jennifer Lising Roxas, V K Viswanathan

Open access · greenAbstract readReview
In one paragraph

Review in Comprehensive Physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Attaching and effacing pathogens modulate host mitochondrial structure and function.International review of cell and molecular biology · 2023
    Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. The role and therapeutic potential of gut microbiome in severe burn.Frontiers in cellular and infection microbiology · 2022
    Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Gut Barrier and Microbiota in Cirrhosis.Journal of clinical and experimental hepatology
    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

2 authors at 1 institution in 1 country.

Jennifer Lising RoxasSchool of Animal and Comparative Biomedical Sciences, University of Arizona, Tucson, Arizona, USA.
V K ViswanathanSchool of Animal and Comparative Biomedical Sciences, University of Arizona, Tucson, Arizona, USA.
University of Arizona · US

Funding

Dynamic Regulation of Epithelial Cell Survival by Enteropathogenic E. coliR01AI081742 · NIAID · UNIVERSITY OF ARIZONA · PI VISWANATHAN, V K · 2011 to 2015
$1.9M
Dynamic regulation of epithelial cell survival by enteropathogenic E. coliR56AI081742 · NIAID · UNIVERSITY OF ARIZONA · PI VISWANATHAN, V K · 2009 to 2009
$252k
NIAID NIH HHS R01 AI081742NIAID NIH HHS R56 AI081742
6 · The paper itself

Abstract

The passive and regulated movement of ions, solutes, and water via spaces between cells of the epithelial monolayer plays a critical role in the normal intestinal functioning. This paracellular pathway displays a high level of structural and functional specialization, with the membrane-spanning complexes of the tight junctions, adherens junctions, and desmosomes ensuring its integrity. Tight junction proteins, like occludin, tricellulin, and the claudin family isoforms, play prominent roles as barriers to unrestricted paracellular transport. The past decade has witnessed major advances in our understanding of the architecture and function of epithelial tight junctions. While it has been long appreciated that microbes, notably bacterial and viral pathogens, target and disrupt junctional complexes and alter paracellular permeability, the precise mechanisms remain to be defined. Notably, renewed efforts will be required to interpret the available data on pathogen-mediated barrier disruption in the context of the most recent findings on tight junction structure and function. While much of the focus has been on pathogen-induced dysregulation of junctional complexes, commensal microbiota and their products may influence paracellular permeability and contribute to the normal physiology of the gut. Finally, microbes and their products have become important tools in exploring host systems, including the junctional properties of epithelial cells. © 2018 American Physiological Society. Compr Physiol 8:823-842, 2018.

Indexed as

AnimalsBacteriaBacterial InfectionsBiological TransportGastrointestinal MicrobiomeHumansIntestinal MucosaPermeabilityTight Junctions

Identifiers

PMID29687905
PMCPMC11617015
OpenAlexW2886290720

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.