Evidence map›Paper›PMID 31847469›Full record

ArticleCells2019

Temporal Dynamics of VEGFA-Induced VEGFR2/FAK Co-Localization Depend on SHB.

Ilkka Pietilä, Djenolan Van Mourik, Andreas Tamelander, Vitezslav Kriz, Lena Claesson-Welsh, Anders Tengholm, Michael Welsh

Open access · goldAbstract read
In one paragraph

Article in Cells, 2019. 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
0.7field-weighted citation impact, top 30% 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, 14 citations in OpenAlex.

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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

7 authors at 2 institutions in 2 countries.

Ilkka PietiläDepartment of Medical Cell Biology, Uppsala University, Box 571, 75123 Uppsala, Sweden.
Djenolan Van MourikDepartment of Medical Cell Biology, Uppsala University, Box 571, 75123 Uppsala, Sweden.
Andreas TamelanderDepartment of Medical Cell Biology, Uppsala University, Box 571, 75123 Uppsala, Sweden.
Vitezslav KrizInstitute of Molecular Genetics of the CAS, 14220 Prague, Czech Republic.
Lena Claesson-WelshDepartment of Immunology, Genetics and Pathology, Uppsala University, 75108 Uppsala, Sweden.
Anders TengholmDepartment of Medical Cell Biology, Uppsala University, Box 571, 75123 Uppsala, Sweden.
Michael WelshDepartment of Medical Cell Biology, Uppsala University, Box 571, 75123 Uppsala, Sweden.ORCID 0000-0002-5467-9755
Uppsala University · SECzech Academy of Sciences, Institute of Molecular Genetics · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Focal adhesion kinase (FAK) is essential for vascular endothelial growth factor-A (VEGFA)/VEGF receptor-2 (VEGFR2)-stimulated angiogenesis and vascular permeability. We have previously noted that presence of the Src homology-2 domain adapter protein B (SHB) is of relevance for VEGFA-stimulated angiogenesis in a FAK-dependent manner. The current study was conducted in order address the temporal dynamics of co-localization between these components in HEK293 and primary lung endothelial cells (EC) by total internal reflection fluorescence microscopy (TIRF). An early (<2.5 min) VEGFA-induced increase in VEGFR2 co-localization with SHB was dependent on tyrosine 1175 in VEGFR2. VEGFA also enhanced SHB co-localization with FAK. FAK co-localization with VEGFR2 was dependent on SHB since it was significantly lower in SHB deficient EC after VEGFA addition. Absence of SHB also resulted in a gradual decline of VEGFR2 co-localization with FAK under basal (prior to VEGFA addition) conditions. A similar basal response was observed with expression of the Y1175F-VEGFR2 mutant in wild type EC. The distribution of focal adhesions in SHB-deficient EC was altered with a primarily perinuclear location. These live cell data implicate SHB as a key component regulating FAK activity in response to VEGFA/VEGFR2.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCell MovementEndothelial CellsFemaleFocal Adhesion Protein-Tyrosine KinasesHEK293 CellsHumansMaleMiceMice, Inbred BALB CMice, KnockoutNeovascularization, PhysiologicProto-Oncogene ProteinsVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2Adaptor Proteins, Signal TransducingFocal Adhesion Protein-Tyrosine KinasesKDR protein, humanKdr protein, mouseProto-Oncogene ProteinsSHB protein, humanVascular Endothelial Growth Factor Avascular endothelial growth factor A, mouseVascular Endothelial Growth Factor Receptor-2VEGFA protein, humanangiogenesisFAKfocal adhesionsSHBTIRFVEGFR2

Identifiers

PMID31847469
PMCPMC6953046
OpenAlexW2995501560

What OpenQuestion holds

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LicenceCC BY
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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.