Evidence map›Paper›PMID 20066090›Full record

ReviewCold Spring Harbor perspectives in biology2009

Physiology and function of the tight junction.

James M Anderson, Christina M Van Itallie

Open access · bronzeAbstract readReview
In one paragraph

Review in Cold Spring Harbor perspectives in biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 562 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
562citing papers in PubMed, 1 pooled it
–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

562 citing papers in PubMed, 1 synthesis or guideline pooled it, 1,015 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Review
  5. Review
  6. Article
  7. Tight junction structure, assembly and (dys)function.Nature reviews. Molecular cell biology · 2026
    Review
  8. Article
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  11. Article
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  19. Review
  20. Review

502 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

2 authors at 1 institution in 1 country.

James M AndersonDepartment of Cell and Molecular Physiology, University of North Carolina at Chapel Hill, 6312 MBRB, Chapel Hill, North Carolina 27599-7545, USA. jandersn@med.unc.edu
Christina M Van Itallie
University of North Carolina at Chapel Hill · US

Funding

PILOT AND FEASIBILITY STUDIESP30DK034987 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ROBERT S. SANDLER · 1985 to 2026
$30.5M
ZO-1 & Cytoplasmic Scaffolding of the Tight JunctionR01DK061397 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FANNING, ALAN SCOTT · 2003 to 2012
$3.4M
Tight Junction Barriers in the Gastrointestinal TractR01DK045134 · NIDDK · YALE UNIVERSITY · PI ANDERSON, JAMES M. · 1992 to 2010
$2.9M
ZO-1 & Cytoplasmic Scaffolding of the Tight JunctionR56DK061397 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ANDERSON, JAMES M. · 2008 to 2008
$327k
NIDDK NIH HHS DK45134NIDDK NIH HHS DK61397NIDDK NIH HHS P30 DK034987NIDDK NIH HHS R01 DK045134NIDDK NIH HHS R01 DK061397NIDDK NIH HHS R56 DK061397
6 · The paper itself

Abstract

Understanding of tight junctions has evolved from their historical perception as inert solute barriers to recognition of their physiological and biochemical complexity. Many proteins are specifically localized to tight junctions, including cytoplasmic actin-binding proteins and adhesive transmembrane proteins. Among the latter are claudins, which are critical barrier proteins. Current information suggests that the paracellular barrier is most usefully modeled as having two physiologic components: a system of charge-selective small pores, 4 A in radius, and a second pathway created by larger discontinuities in the barrier, lacking charge or size discrimination. The first pathway is influenced by claudin expression patterns and the second is likely controlled by different proteins and signals. Recent information on claudin function and disease-causing mutations have led to a more complete understanding of their role in barrier formation, but progress is impeded by lack of high resolution structural information.

Indexed as

Amino Acid SequenceAnimalsBiological TransportCell MembraneClaudinsCytoplasmElectrophysiologyGenetic Predisposition to DiseaseHumansModels, BiologicalMolecular Sequence DataSequence Homology, Amino AcidTight JunctionsClaudins

Identifiers

PMID20066090
PMCPMC2742087
OpenAlexW2101976554

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.