Evidence map›Paper›PMID 42343561›Full record

ArticleBiophysical journal2026

Cryo-electron tomography reveals paracellular claudin-15 pores at the tight junction.

Evgeniya A Demchenko, Sarah McGuinness, Shaun Wood, Joseph Kainov, Victoria Pappas, Jotham Austin, Dominic Hyatt, Fatemeh Khalili-Araghi, Le Shen, Christopher R Weber

Abstract read
In one paragraph

Article in Biophysical journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Evgeniya A DemchenkoDepartment of Biochemistry and Molecular Biology, The University of Chicago, Chicago, IL, USA; Center for Mechanical Excitability, The University of Chicago, Chicago, IL, USA.
Sarah McGuinnessDepartment of Biomedical Engineering, University of Illinois Chicago, Chicago, IL, USA; Department of Physics, University of Illinois Chicago, Chicago, IL, USA.
Shaun WoodDepartment of Pathology, The University of Chicago, Chicago, IL, USA.
Joseph KainovDepartment of Pathology, The University of Chicago, Chicago, IL, USA.
Victoria PappasAdvanced Electron Microscopy Core, The University of Chicago, Chicago, IL, USA.
Jotham AustinAdvanced Electron Microscopy Core, The University of Chicago, Chicago, IL, USA.
Dominic HyattDepartment of Pathology, The University of Chicago, Chicago, IL, USA.
Fatemeh Khalili-AraghiDepartment of Physics, University of Illinois Chicago, Chicago, IL, USA. Electronic address: akhalili@uic.edu.
Le ShenDepartment of Pathology, The University of Chicago, Chicago, IL, USA; Department of Surgery, The University of Chicago, Chicago, IL, USA. Electronic address: leshen@uchicago.edu.
Christopher R WeberDepartment of Pathology, The University of Chicago, Chicago, IL, USA. Electronic address: cweber@bsd.uchicago.edu.

Funding

Structure, function, and modulation of claudin cation channels in the GI tractR01DK131542 · NIDDK · UNIVERSITY OF CHICAGO · PI KHALILI-ARAGHI, FATEMEH, WEBER, CHRISTOPHER · 2021 to 2025
$2.5M
NIDDK NIH HHS R01 DK131542
6 · The paper itself

Abstract

Tight junctions (TJs) within simple epithelia are composed of networks of anastomosing strands at the apical end of the intercellular space. Members of the claudin family of proteins reside within TJ strands and either seal the paracellular space or assemble into charge and size-selective pathways. Functional studies suggest that claudin-mediated conductance pathways resemble traditional ion channels. However, postulated pores have not been directly visualized. Using claudin-deficient epithelia in which exogenously introduced EGFP-CLDN15 is the principal claudin family member expressed, our investigation sheds light on the arrangement and structure of the putative claudin pores. Following correlative light and electron microscopy identification of TJs and cryo-electron tomography, we identified a series of linearly distributed electron-lucent features located between two closely apposed plasma membranes of adjacent cells. In contrast, such features were not observed in claudin-deficient epithelia with exogenous mCherry-ZO-1 expression. Morphometric analyses showed the median diameter of these features is 1.5 nm, with a median distance between adjacent features of 2.3 nm. These findings agree with the postulated and extensively modeled claudin pores formed within simple epithelia. This provides the first direct evidence of paracellular claudin pore organization and paves the way for future biophysical investigations.

Indexed as

ClaudinsCryoelectron MicroscopyElectron Microscope TomographyTight JunctionsAnimalsDogsclaudin 15Claudins

Identifiers

PMID42343561
PMCPMC13507467

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.