Evidence map›Paper›PMID 26539695›Full record

ArticleGlia2016

Astrocytes spatially restrict VEGF signaling by polarized secretion and incorporation of VEGF into the actively assembling extracellular matrix.

Kristof Egervari, Gael Potter, Maria Luisa Guzman-Hernandez, Patrick Salmon, Martinho Soto-Ribeiro, Birgit Kastberger, Tamas Balla, Bernhard Wehrle-Haller, Jozsef Zoltan Kiss

Open access · greenAbstract read
In one paragraph

Article in Glia, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. The Role of Astrocytes in the Neurorepair Process.Frontiers in cell and developmental biology · 2021
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. 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

9 authors at 4 institutions in 2 countries.

Kristof EgervariDepartment of Neurosciences, University of Geneva, Switzerland.
Gael PotterDepartment of Neurosciences, University of Geneva, Switzerland.
Maria Luisa Guzman-HernandezSection on Molecular Signal Transduction, Program for Developmental Neuroscience, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland.
Patrick SalmonDepartment of Neurosciences, University of Geneva, Switzerland.
Martinho Soto-RibeiroDepartment of Cell Physiology and Metabolism, University of Geneva, Switzerland.
Birgit KastbergerDepartment of Cell Physiology and Metabolism, University of Geneva, Switzerland.
Tamas BallaSection on Molecular Signal Transduction, Program for Developmental Neuroscience, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland.
Bernhard Wehrle-HallerDepartment of Cell Physiology and Metabolism, University of Geneva, Switzerland.
Jozsef Zoltan KissDepartment of Neurosciences, University of Geneva, Switzerland.
University of Geneva · CHEunice Kennedy Shriver National Institute of Child Health and Human Development · USNational Institutes of Health · USUniversity Hospital of Geneva · CH

Funding

Phosphoinositide-calcium Signaling In Cell RegulationZIAHD000196 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI BALLA, TAMAS · 2009 to 2025
$26.3M
PHOSPHOINOSITIDE-CALCIUM SIGNALING IN CELL REGULATIONZ01HD000196 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI BALLA, TAMAS · 1998 to 2008
$1.9M
Intramural NIH HHS Z01 HD000196
6 · The paper itself

Abstract

The spatial organization of vascular endothelial growth factor (VEGF) signaling is a key determinant of vascular patterning during development and tissue repair. How VEGF signaling becomes spatially restricted and the role of VEGF secreting astrocytes in this process remains poorly understood. Using a VEGF-GFP fusion protein and confocal time-lapse microscopy, we observed the intracellular routing, secretion and immobilization of VEGF in scratch-activated living astrocytes. We found VEGF to be directly transported to cell-extracellular matrix attachments where it is incorporated into fibronectin fibrils. VEGF accumulated at β1 integrin containing fibrillar adhesions and was translocated along the cell surface prior to internalization and degradation. We also found that only the astrocyte-derived, matrix-bound, and not soluble VEGF decreases β1 integrin turnover in fibrillar adhesions. We suggest that polarized VEGF release and ECM remodeling by VEGF secreting cells is key to control the local concentration and signaling of VEGF. Our findings highlight the importance of astrocytes in directing VEGF functions and identify these mechanisms as promising target for angiogenic approaches.

Indexed as

AnimalsAstrocytesCell PolarityCells, CulturedCerebral CortexExtracellular MatrixGreen Fluorescent ProteinsHydrazonesKi-67 AntigenMicroscopy, ConfocalNeuronsPhotobleachingPuromycinRatsRats, WistarSignal TransductionGreen Fluorescent ProteinsHydrazonesKi-67 AntigenN'-(3,4-dihydroxybenzylidene)-3-hydroxy-2-naphthahydrazidePuromycinSoluble N-Ethylmaleimide-Sensitive Factor Attachment ProteinsVascular Endothelial Growth Factor Aextracellular matrixfibrillar adhesionfibronectingrowth factor signaling

Identifiers

PMID26539695
PMCPMC6615037
OpenAlexW2158231047

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.