Evidence map›Paper›PMID 37750425›Full record

ArticleMicrocirculation (New York, N.Y. : 1994)2023

Arf6 is required for endocytosis and filamentous actin assembly during angiogenesis in vitro.

Caitlin R Francis, Makenzie L Bell, Marina M Skripnichuk, Erich J Kushner

Open access · greenAbstract read
In one paragraph

Article in Microcirculation (New York, N.Y. : 1994), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. SARS-CoV-2 uptake and inflammatory response in senescent endothelial cells are regulated by the BSG/VEGFR2 pathway.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
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  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Caitlin R FrancisDepartment of Biological Sciences, University of Denver, Denver, Colorado, USA.
Makenzie L BellDepartment of Biological Sciences, University of Denver, Denver, Colorado, USA.
Marina M SkripnichukDepartment of Biological Sciences, University of Denver, Denver, Colorado, USA.
Erich J KushnerDepartment of Biological Sciences, University of Denver, Denver, Colorado, USA.ORCID 0000-0002-1355-9511
University of Denver · US

Funding

Polarized Protein Trafficking and AngiogenesisR01HL155921 · NHLBI · UNIVERSITY OF DENVER (COLORADO SEMINARY) · PI Erich J Kushner · 2022 to 2026
$1.8M
Mechanisms of Delta-like 4 Endocytosis and Notch Activation During Blood Vessel DevelopmentR15HL156106 · NHLBI · UNIVERSITY OF DENVER (COLORADO SEMINARY) · PI KUSHNER, ERICH J · 2021 to 2021
$439k
NHLBI NIH HHS R01 HL155921NHLBI NIH HHS R01HL155921-01A1NHLBI NIH HHS R15 HL156106NHLBI NIH HHS R15HL156106-01A1
6 · The paper itself

Abstract

objectiveEndocytosis is a process vital to angiogenesis and vascular homeostasis. In pathologies where supraphysiological growth factor signaling underlies disease etiology, such as in diabetic retinopathy and solid tumors, strategies to limit chronic growth factor signaling by way of blunting endocytic processes have been shown to have tremendous clinical value. ADP ribosylation factor 6 (Arf6) is a small GTPase that promotes the assembly of actin necessary for clathrin-mediated and clathrin-independent endocytosis. In its absence, growth factor signaling is greatly diminished, which has been shown to ameliorate pathological signaling input in diseased vasculature. However, it is less clear if there are bystander effects related to loss of Arf6 on angiogenic behaviors. Our goal was to provide an analysis of Arf6's function in angiogenic endothelium, focusing on its role in actin and endocytosis as well as sprouting morphogenesis.

methodsPrimary endothelial cells were cultured in both 2D and 3D environments. Here, endothelial cells were fixed and stained for various proteins or transfected with fluorescently-tagged constructs for live-cell imaging.

resultsWe found that Arf6 localized to both filamentous actin and sites of endocytosis in two-dimensional culture. Loss of Arf6 distorted both apicobasal polarity and reduced the total cellular filamentous actin content, which may be the primary driver underlying gross sprouting dysmorphogenesis in its absence.

conclusionsOur findings highlight that endothelial Arf6 is a potent mediator of both actin regulation and endocytosis and is required for proper sprout formation.

Indexed as

ActinsADP-Ribosylation Factor 6ADP-Ribosylation FactorsClathrinEndocytosisEndothelial CellsIntercellular Signaling Peptides and ProteinsActinsADP-Ribosylation Factor 6ADP-Ribosylation FactorsClathrinIntercellular Signaling Peptides and ProteinsACAP2actinangiogenesisArf6ARNOblood vessel developmentclathrin-mediated endocytosisGAPGEFlumenogenesis

Identifiers

PMID37750425
PMCPMC10688150
OpenAlexW4387033272

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.