Evidence map›Paper›PMID 39129490›Full record

ReviewAmerican journal of physiology. Cell physiology2024

Junctions at the crossroads: the impact of mechanical cues on endothelial cell-cell junction conformations and vascular permeability.

Ken D Brandon, William E Frank, Kimberly M Stroka

Abstract readReview
In one paragraph

Review in American journal of physiology. Cell physiology, 2024. 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.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Matrix stiffness induces endothelial network senescence.bioRxiv : the preprint server for biology · 2025
    Article
  13. Article
  14. Article
  15. The vascular endothelium as decision maker in lung injury.Frontiers in cell and developmental biology · 2025
    Review
  16. Review
  17. Review
  18. Advancements and future directions inAmerican journal of physiology. Cell physiology · 2024
    Article
  19. 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

3 authors.

Ken D BrandonFischell Department of Bioengineering, University of Maryland, College Park, Maryland, United States.
William E FrankDepartment of Biology, University of Puerto Rico in Ponce, Ponce, Puerto Rico.
Kimberly M StrokaFischell Department of Bioengineering, University of Maryland, College Park, Maryland, United States.ORCID 0000-0003-3314-2067

Funding

University of Maryland Summer Training and Research (UM STAR) ProgramR25HL092604 · NHLBI · UNIV OF MARYLAND, COLLEGE PARK · PI HAGBERG, JAMES M · 2008 to 2024
$1.6M
Clark School of Engineering Clark Doctoral FellowshipHHS | National Institutes of Health (NIH) 5R25HL092604-14National Science Foundation (NSF) 1944121NHLBI NIH HHS R25 HL092604
6 · The paper itself

Abstract

Cells depend on precisely regulating barrier function within the vasculature to maintain physiological stability and facilitate essential substance transport. Endothelial cells achieve this through specialized adherens and tight junction protein complexes, which govern paracellular permeability across vascular beds. Adherens junctions, anchored by vascular endothelial (VE)-cadherin and associated catenins to the actin cytoskeleton, mediate homophilic adhesion crucial for barrier integrity. In contrast, tight junctions composed of occludin, claudin, and junctional adhesion molecule A interact with Zonula Occludens proteins, reinforcing intercellular connections essential for barrier selectivity. Endothelial cell-cell junctions exhibit dynamic conformations during development, maturation, and remodeling, regulated by local biochemical and mechanical cues. These structural adaptations play pivotal roles in disease contexts such as chronic inflammation, where junctional remodeling contributes to increased vascular permeability observed in conditions from cancer to cardiovascular diseases. Conversely, the brain microvasculature's specialized junctional arrangements pose challenges for therapeutic drug delivery due to their unique molecular compositions and tight organization. This commentary explores the molecular mechanisms underlying endothelial cell-cell junction conformations and their implications for vascular permeability. By highlighting recent advances in quantifying junctional changes and understanding mechanotransduction pathways, we elucidate how physical forces from cellular contacts and hemodynamic flow influence junctional dynamics.

Indexed as

Capillary PermeabilityEndothelial CellsMechanotransduction, CellularTight JunctionsAdherens JunctionsAnimalsHumansIntercellular Junctionscell-cell junction conformationsendothelial cellsmechanical forcespermeabilityVE-cadherin

Identifiers

PMID39129490
PMCPMC11481987

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.