Evidence map›Paper›PMID 28949796›Full record

ArticleSmall GTPases2019

RhoA, RhoB and RhoC differentially regulate endothelial barrier function.

Manon C A Pronk, Jan S M van Bezu, Geerten P van Nieuw Amerongen, Victor W M van Hinsbergh, Peter L Hordijk

Open access · hybridAbstract read
In one paragraph

Article in Small GTPases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

35 citing papers in PubMed, 84 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. The machinery of healthy vasoconstriction: an overview.Pflugers Archiv : European journal of physiology · 2025
    Review
  6. Article
  7. Time-course transcriptomics reveals the impact ofFrontiers in microbiology · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Small Extracellular Vesicles Propagate the Inflammatory Response After Trauma.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    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

5 authors at 1 institution in 1 country.

Manon C A PronkDepartment of Physiology, VU University Medical Center Amsterdam , Amsterdam , The Netherlands.ORCID 0000-0002-2235-1683
Jan S M van BezuDepartment of Physiology, VU University Medical Center Amsterdam , Amsterdam , The Netherlands.
Geerten P van Nieuw AmerongenDepartment of Physiology, VU University Medical Center Amsterdam , Amsterdam , The Netherlands.
Victor W M van HinsberghDepartment of Physiology, VU University Medical Center Amsterdam , Amsterdam , The Netherlands.
Peter L HordijkDepartment of Physiology, VU University Medical Center Amsterdam , Amsterdam , The Netherlands.
Amsterdam UMC Location Vrije Universiteit Amsterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RhoGTPases are known regulators of intracellular actin dynamics that are important for maintaining endothelial barrier function. RhoA is most extensively studied as a key regulator of endothelial barrier function, however the function of the 2 highly homologous family-members (> 88%) RhoB and RhoC in endothelial barrier function is still poorly understood. This study aimed to determine whether RhoA, RhoB and RhoC have overlapping or distinct roles in barrier function and permeability in resting and activated endothelium. By using primary endothelial cells in combination with siRNA transfection to establish individual, double or triple knockdown of the RhoA/B/C RhoGTPases, we found that RhoB, but not RhoA or RhoC, is in resting endothelium a negative regulator of permeability. Loss of RhoB accounted for an accumulation of VE-cadherin at cell-cell contacts. Thrombin-induced loss of endothelial integrity is mediated primarily by RhoA and RhoB. Combined loss of RhoA/B showed decreased phosphorylation of Myosin Light Chain and increased expression of VE-cadherin at cell-cell contacts after thrombin stimulation. RhoC contributes to the Rac1-dependent restoration of endothelial barrier function. In summary, this study shows that these highly homologous RhoGTPases differentially control the dynamics of endothelial barrier function.

Indexed as

ActinsAntigens, CDCadherin 5CadherinsCell CommunicationCells, CulturedHumansHuman Umbilical Vein Endothelial Cellsrac1 GTP-Binding ProteinrhoA GTP-Binding ProteinrhoB GTP-Binding ProteinrhoC GTP-Binding ProteinRNA, Small InterferingThrombinActinsAntigens, CDCadherin 5Cadherinsrac1 GTP-Binding ProteinRAC1 protein, humanrhoA GTP-Binding ProteinRHOA protein, humanrhoB GTP-Binding ProteinRHOB protein, humanrhoC GTP-Binding ProteinRHOC protein, humanRNA, Small InterferingThrombincytoskeletonEndothelial barrier functionRhoARhoBRhoCRhoGTPasesVE-cadherin

Identifiers

PMID28949796
PMCPMC6748378
OpenAlexW2759945688

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.