Evidence map›Paper›PMID 25249937›Full record

ArticleFrontiers in cellular neuroscience2014

In vivo bioluminescence imaging of vascular remodeling after stroke.

Joanna M Adamczak, Gabriele Schneider, Melanie Nelles, Ivo Que, Ernst Suidgeest, Louise van der Weerd, Clemens Löwik, Mathias Hoehn

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Neural Stem Cells for Early Ischemic Stroke.International journal of molecular sciences · 2021
    Review
  5. Review
  6. Impact of High Salt Diet on Cerebral Vascular Function and Stroke inInternational journal of molecular sciences · 2019
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Sensorimotor Functional and Structural Networks after Intracerebral Stem Cell Grafts in the Ischemic Mouse Brain.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  12. Dynamic Modulation of Microglia/Macrophage Polarization by miR-124 after Focal Cerebral Ischemia.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2016
    Article
  13. 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

8 authors at 2 institutions in 2 countries.

Joanna M AdamczakIn-vivo-NMR Laboratory, Max-Planck-Institute for Neurological Research Cologne, Germany.
Gabriele SchneiderIn-vivo-NMR Laboratory, Max-Planck-Institute for Neurological Research Cologne, Germany.
Melanie NellesIn-vivo-NMR Laboratory, Max-Planck-Institute for Neurological Research Cologne, Germany.
Ivo QueDepartment of Endocrinology, Leiden University Medical Center Leiden, Netherlands.
Ernst SuidgeestDepartment of Radiology, Leiden University Medical Center Leiden, Netherlands.
Louise van der WeerdDepartment of Radiology, Leiden University Medical Center Leiden, Netherlands ; Department of Human Genetics, Leiden University Medical Center Leiden, Netherlands.
Clemens LöwikDepartment of Endocrinology, Leiden University Medical Center Leiden, Netherlands ; Department of Radiology, Leiden University Medical Center Leiden, Netherlands.
Mathias HoehnIn-vivo-NMR Laboratory, Max-Planck-Institute for Neurological Research Cologne, Germany ; Department of Radiology, Leiden University Medical Center Leiden, Netherlands.
Leiden University Medical Center · NLMax Planck Institute for Metabolism Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thrombolysis remains the only beneficial therapy for ischemic stroke, but is restricted to a short therapeutic window following the infarct. Currently research is focusing on spontaneous regenerative processes during the sub-acute and chronic phase. Angiogenesis, the formation of new blood vessels from pre-existing ones, was observed in stroke patients, correlates with longer survival and positively affects the formation of new neurons. Angiogenesis takes place in the border zones of the infarct, but further insight into the temporal profile is needed to fully apprehend its therapeutic potential and its relevance for neurogenesis and functional recovery. Angiogenesis is a multistep process, involving extracellular matrix degradation, endothelial cell proliferation, and, finally, new vessel formation. Interaction between vascular endothelial growth factor and its receptor 2 (VEGFR2) plays a central role in these angiogenic signaling cascades. In the present study we investigated non-invasively the dynamics of VEGFR2 expression following cerebral ischemia in a mouse model of middle cerebral artery occlusion (MCAO). We used a transgenic mouse expressing firefly luciferase under the control of the VEGFR2 promotor to non-invasively elucidate the temporal profile of VEGFR2 expression after stroke as a biomarker for VEGF/VEGFR2 signaling. We measured each animal repetitively up to 2 weeks after stroke and found increased VEGFR2 expression starting 3 days after the insult with peak values at 7 days. These were paralleled by increased VEGFR2 protein levels and increased vascular volume in peri-infarct areas at 14 days after the infarct, indicating that signaling via VEGFR2 leads to successful vascular remodeling. This study describes VEGFR2-related signaling is active at least up to 2 weeks after the infarct and results in increased vascular volume. Further, this study presents a novel strategy for the non-invasive evaluation of angiogenesis-based therapies.

Indexed as

angiogenesiscerebral ischemiaflk-1VEGFR2vessel density

Identifiers

PMID25249937
PMCPMC4155794
OpenAlexW2052485863

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.