Evidence map›Paper›PMID 31162891›Full record

ArticleActa physiologica (Oxford, England)2020

AKAP12 deficiency impairs VEGF-induced endothelial cell migration and sprouting.

Peter M Benz, Yindi Ding, Heike Stingl, Annemarieke E Loot, Joana Zink, Ilka Wittig, Rüdiger Popp, Ingrid Fleming

Open access · hybridAbstract read
In one paragraph

Article in Acta physiologica (Oxford, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

30 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
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  3. FPR1-dependent Pro-inflammatory Ccl4Respiratory research · 2025
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  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. The scaffolding protein AKAP12 regulates mRNA localization and translation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Role of A-Kinase Anchoring Protein 12 in the Central Nervous System.Journal of clinical neurology (Seoul, Korea) · 2023
    Review
  16. TheMolecular biology of the cell · 2023
    Article
  17. Review
  18. Review
  19. 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.

Peter M BenzInstitute for Vascular Signalling, Centre for Molecular Medicine, Goethe University, Frankfurt am Main, Germany.
Yindi DingInstitute for Vascular Signalling, Centre for Molecular Medicine, Goethe University, Frankfurt am Main, Germany.
Heike StinglInstitute for Vascular Signalling, Centre for Molecular Medicine, Goethe University, Frankfurt am Main, Germany.
Annemarieke E LootInstitute for Vascular Signalling, Centre for Molecular Medicine, Goethe University, Frankfurt am Main, Germany.
Joana ZinkInstitute for Vascular Signalling, Centre for Molecular Medicine, Goethe University, Frankfurt am Main, Germany.
Ilka WittigGerman Center of Cardiovascular Research (DZHK), Partner site RheinMain, Frankfurt am Main, Germany.
Rüdiger PoppInstitute for Vascular Signalling, Centre for Molecular Medicine, Goethe University, Frankfurt am Main, Germany.
Ingrid FlemingInstitute for Vascular Signalling, Centre for Molecular Medicine, Goethe University, Frankfurt am Main, Germany.ORCID 0000-0003-1881-3635
Goethe University Frankfurt · DE

Funding

Deutsche Forschungsgemeinschaft "Exzellenzcluster 147 "Cardio-Pulmonary Systems"Deutsche Forschungsgemeinschaft SFB 815/3 Z1Deutsche Forschungsgemeinschaft SFB 834/1 A4Deutsche Forschungsgemeinschaft SFB 834/2 A8
6 · The paper itself

Abstract

aimProtein kinase (PK) A anchoring protein (AKAP) 12 is a scaffolding protein that anchors PKA to compartmentalize cyclic AMP signalling. This study assessed the consequences of the downregulation or deletion of AKAP12 on endothelial cell migration and angiogenesis.

methodsThe consequences of siRNA-mediated downregulation AKAP12 were studied in primary cultures of human endothelial cells as well as in endothelial cells and retinas from wild-type versus AKAP12

resultsAKAP12 was expressed at low levels in confluent endothelial cells but its expression was increased in actively migrating cells, where it localized to lamellipodia. In the postnatal retina, AKAP12 was expressed by actively migrating tip cells at the angiogenic front, and its deletion resulted in defective extension of the vascular plexus. In migrating endothelial cells, AKAP12 was co-localized with the PKA type II-α regulatory subunit as well as multiple key regulators of actin dynamics and actin filament-based movement; including components of the Arp2/3 complex and the vasodilator-stimulated phosphoprotein (VASP). Fitting with the evidence of a physical VASP/AKAP12/PKA complex, it was possible to demonstrate that the VEGF-stimulated and PKA-dependent phosphorylation of VASP was dependent on AKAP12. Indeed, AKAP12 colocalized with phospho-Ser157 VASP at the leading edge of migrating endothelial cells.

conclusionThe results suggest that compartmentalized AKAP12/PKA signalling mediates VASP phosphorylation at the leading edge of migrating endothelial cells to translate angiogenic stimuli into altered actin dynamics and cell movement.

Indexed as

A Kinase Anchor ProteinsAnimalsCell Adhesion MoleculesCell Cycle ProteinsCell MovementCyclic AMP-Dependent Protein KinasesEndothelial CellsGene Expression RegulationMiceMice, KnockoutMicrofilament ProteinsPhosphoproteinsPhosphorylationVascular Endothelial Growth Factor AVasodilator-Stimulated PhosphoproteinAkap12 protein, mouseA Kinase Anchor ProteinsCell Adhesion MoleculesCell Cycle ProteinsCyclic AMP-Dependent Protein KinasesMicrofilament ProteinsPhosphoproteinsVascular Endothelial Growth Factor AVasodilator-Stimulated Phosphoproteinangiogenesisprotein kinase Aprotein kinase A anchoring protein 12retinavasodilator-stimulated phosphoprotein

Identifiers

PMID31162891
PMCPMC6916389
OpenAlexW2948163554

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.