Evidence map›Paper›PMID 29358211›Full record

ArticleThe Journal of cell biology2018

The Cullin-3-Rbx1-KCTD10 complex controls endothelial barrier function via K63 ubiquitination of RhoB.

Igor Kovačević, Tomohisa Sakaue, Jisca Majoleé, Manon C Pronk, Masashi Maekawa, Dirk Geerts, Mar Fernandez-Borja, Shigeki Higashiyama, Peter L Hordijk

Open access · greenAbstract read
In one paragraph

Article in The Journal of cell biology, 2018. 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
2.6field-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, 57 citations in OpenAlex.

  1. Article
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  6. Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  7. Article
  8. Article
  9. The CRL3Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Regulation of the water channel aquaporin-2 by cullin E3 ubiquitin ligases.American journal of physiology. Renal physiology · 2024
    Article
  11. KCTD10 regulates brain development by destabilizing brain disorder-associated protein KCTD13.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Mechanical stress shapes the cancer cell response to neddylation inhibition.Journal of experimental & clinical cancer research : CR · 2022
    Article
  17. Review
  18. Review
  19. Article
  20. The emerging role of the KCTD proteins in cancer.Cell communication and signaling : CCS · 2021
    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

9 authors at 4 institutions in 2 countries.

Igor KovačevićDepartment of Molecular Cell Biology, Sanquin Research, Amsterdam, Netherlands.ORCID 0000-0003-1834-2378
Tomohisa SakaueDivision of Cell Growth and Tumor Regulation, Proteo-Science Center, Ehime University, Toon, Ehime, Japan.
Jisca MajoleéDepartment of Molecular Cell Biology, Sanquin Research, Amsterdam, Netherlands.ORCID 0000-0003-4450-3948
Manon C PronkDepartment of Physiology, Vrije Universiteit University Medical Center, Amsterdam, Netherlands.ORCID 0000-0002-2235-1683
Masashi MaekawaDivision of Cell Growth and Tumor Regulation, Proteo-Science Center, Ehime University, Toon, Ehime, Japan.ORCID 0000-0002-9574-1906
Dirk GeertsDepartment of Pediatric Oncology/Hematology, Erasmus University Medical Center, Rotterdam, Netherlands.ORCID 0000-0002-6386-8187
Mar Fernandez-BorjaDepartment of Molecular Cell Biology, Sanquin Research, Amsterdam, Netherlands.ORCID 0000-0002-1503-433X
Shigeki HigashiyamaDivision of Cell Growth and Tumor Regulation, Proteo-Science Center, Ehime University, Toon, Ehime, Japan shigeki@m.ehime-u.ac.jp.
Peter L HordijkDepartment of Physiology, Vrije Universiteit University Medical Center, Amsterdam, Netherlands p.hordijk@vumc.nl.ORCID 0000-0002-3348-078X
Ehime University · JPSanquin · NLVrije Universiteit Amsterdam · NLErasmus MC · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RhoGTPases control endothelial cell (EC) migration, adhesion, and barrier formation. Whereas the relevance of RhoA for endothelial barrier function is widely accepted, the role of the RhoA homologue RhoB is poorly defined. RhoB and RhoA are 85% identical, but RhoB's subcellular localization and half-life are uniquely different. Here, we studied the role of ubiquitination for the function and stability of RhoB in primary human ECs. We show that the K63 polyubiquitination at lysine 162 and 181 of RhoB targets the protein to lysosomes. Moreover, we identified the RING E3 ligase complex Cullin-3-Rbx1-KCTD10 as key modulator of endothelial barrier integrity via its regulation of the ubiquitination, localization, and activity of RhoB. In conclusion, our data show that ubiquitination controls the subcellular localization and lysosomal degradation of RhoB and thereby regulates the stability of the endothelial barrier through control of RhoB-mediated EC contraction.

Indexed as

UbiquitinationCarrier ProteinsCullin ProteinsHumansHuman Umbilical Vein Endothelial CellsPotassium Channels, Voltage-GatedrhoB GTP-Binding ProteinCarrier ProteinsCUL3 protein, humanCullin ProteinsKCTD10 protein, humanPotassium Channels, Voltage-GatedRBX1 protein, humanrhoB GTP-Binding Protein

Identifiers

PMID29358211
PMCPMC5839774
OpenAlexW2784591516

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.