Evidence map›Paper›PMID 36212522›Full record

ArticleNature cardiovascular research2022

Syndecan-2 selectively regulates VEGF-induced vascular permeability.

F Corti, E Ristori, F Rivera-Molina, D Toomre, J Zhang, J Mihailovic, Z W Zhuang, M Simons

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Nature cardiovascular research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  11. Syndecans modulate ghrelin receptor signaling.Journal of molecular endocrinology · 2025
    Article
  12. Article
  13. Syndecans in hematopoietic cells and their niches.American journal of physiology. Cell physiology · 2024
    Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Activin A Limits VEGF-Induced Permeability via VE-PTP.International journal of molecular sciences · 2023
    Article
  19. KIF13B mediates VEGFR2 recycling to modulate vascular permeability.Cellular and molecular life sciences : CMLS · 2023
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

F CortiYale Cardiovascular Research Center Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06511, USA.
E RistoriYale Cardiovascular Research Center Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06511, USA.
F Rivera-MolinaDepartment of Cell Biology, Yale University School of Medicine, New Haven, CT 06511, USA.
D ToomreDepartment of Cell Biology, Yale University School of Medicine, New Haven, CT 06511, USA.
J ZhangYale Cardiovascular Research Center Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06511, USA.
J MihailovicDepartment of Radiology, Yale University School of Medicine, New Haven, CT 06511, USA.
Z W ZhuangYale Cardiovascular Research Center Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06511, USA.
M SimonsYale Cardiovascular Research Center Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06511, USA.
Yale University · US

Funding

Yale Diabetes Research CenterP30DK045735 · NIDDK · YALE UNIVERSITY · PI Kevan C Herold, GERALD I SHULMAN · 1993 to 2026
$44.0M
Surgery / Physiology CoreP01HL107205 · NHLBI · YALE UNIVERSITY · PI SIMONS, MICHAEL · 2012 to 2022
$18.8M
SYNDECAN FUNCTION IN ENDOTHELIAL CELLSR01HL062289 · NHLBI · YALE UNIVERSITY · PI SIMONS, MICHAEL · 1999 to 2021
$9.6M
Dynamic control of vascular permeability in development and diseaseR01HL149343 · NHLBI · YALE UNIVERSITY · PI EICHMANN, ANNE CHRISTINE, SIMONS, MICHAEL · 2019 to 2022
$3.3M
NHLBI NIH HHS P01 HL107205NHLBI NIH HHS R01 HL062289NHLBI NIH HHS R01 HL149343NIDDK NIH HHS P30 DK045735
6 · The paper itself

Abstract

Vascular endothelial growth factor (VEGF)- driven increase in vascular permeability is a key feature of many disease states associated with inflammation and ischemic injury, contributing significantly to morbidity and mortality in these settings. Despite its importance, no specific regulators that preferentially control VEGF-dependent increase in permeability versus its other biological activities, have been identified. Here we report that a proteoglycan Syndecan-2 (Sdc2) regulates the interaction between a transmembrane phosphatase DEP1 and VEGFR2 by controlling cell surface levels of DEP1. In the absence of Sdc2 or the presence of an antibody that blocks Sdc2-DEP1 interaction, increased plasma membrane DEP1 levels promote selective dephosphorylation of the VEGFR2 Y951 site that is involved in permeability control. Either an endothelial-specific Sdc2 deletion or a treatment with an anti-Sdc2 antibody result in a highly significant reduction in stroke size due to a decrease in intracerebral edema.

Identifiers

PMID36212522
PMCPMC9544384
OpenAlexW4280550846

What OpenQuestion holds

Textmetadata
LicenceTDM
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.