Evidence map›Paper›PMID 32332107›Full record

ArticleMolecular & cellular proteomics : MCP2020

Flow-induced Reorganization of Laminin-integrin Networks Within the Endothelial Basement Membrane Uncovered by Proteomics.

Eelke P Béguin, Esmée F J Janssen, Mark Hoogenboezem, Alexander B Meijer, Arie J Hoogendijk, Maartje van den Biggelaar

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 25 citations in OpenAlex.

  1. Nuclear m6A Methylase METTL3 Drives Production of ITGβ4E to Exacerbate Heart Failure via SRSF3-Mediated Alternative Splicing of ITGβ4.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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  8. Integrin α6 Targeted Tumor Theranostics.Phenomics (Cham, Switzerland) · 2025
    Review
  9. Article
  10. Insight into the Regulation of NDRG1 Expression.International journal of molecular sciences · 2025
    Review
  11. Article
  12. Article
  13. Signal Transduction and Gene Regulation in the Endothelium.Cold Spring Harbor perspectives in medicine · 2023
    Review
  14. Article
  15. Article
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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

6 authors at 1 institution in 1 country.

Eelke P BéguinDepartment of Molecular and Cellular Hemostasis, Sanquin Research, Amsterdam, The Netherlands.
Esmée F J JanssenDepartment of Molecular and Cellular Hemostasis, Sanquin Research, Amsterdam, The Netherlands.
Mark HoogenboezemDepartment of Molecular and Cellular Hemostasis, Sanquin Research, Amsterdam, The Netherlands.
Alexander B MeijerDepartment of Molecular and Cellular Hemostasis, Sanquin Research, Amsterdam, The Netherlands; Department of Biomolecular Mass Spectrometry, Utrecht Institute for Pharmaceutical Sciences (UIPS), Utrecht University, Utrecht, The Netherlands.
Arie J HoogendijkDepartment of Molecular and Cellular Hemostasis, Sanquin Research, Amsterdam, The Netherlands.
Maartje van den BiggelaarDepartment of Molecular and Cellular Hemostasis, Sanquin Research, Amsterdam, The Netherlands. Electronic address: m.vandenbiggelaar@sanquin.nl.
Sanquin · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The vessel wall is continuously exposed to hemodynamic forces generated by blood flow. Endothelial mechanosensors perceive and translate mechanical signals via cellular signaling pathways into biological processes that control endothelial development, phenotype and function. To assess the hemodynamic effects on the endothelium on a system-wide level, we applied a quantitative mass spectrometry approach combined with cell surface chemical footprinting. SILAC-labeled endothelial cells were subjected to flow-induced shear stress for 0, 24 or 48 h, followed by chemical labeling of surface proteins using a non-membrane permeable biotin label, and analysis of the whole proteome and the cell surface proteome by LC-MS/MS analysis. These studies revealed that of the >5000 quantified proteins 104 were altered, which were highly enriched for extracellular matrix proteins and proteins involved in cell-matrix adhesion. Cell surface proteomics indicated that LAMA4 was proteolytically processed upon flow-exposure, which corresponded to the decreased LAMA4 mass observed on immunoblot. Immunofluorescence microscopy studies highlighted that the endothelial basement membrane was drastically remodeled upon flow exposure. We observed a network-like pattern of LAMA4 and LAMA5, which corresponded to the localization of laminin-adhesion molecules ITGA6 and ITGB4. Furthermore, the adaptation to flow-exposure did not affect the inflammatory response to tumor necrosis factor α, indicating that inflammation and flow trigger fundamentally distinct endothelial signaling pathways with limited reciprocity and synergy. Taken together, this study uncovers the blood flow-induced remodeling of the basement membrane and stresses the importance of the subendothelial basement membrane in vascular homeostasis.

Indexed as

Blood CirculationBasement MembraneCells, CulturedChromatography, LiquidEndothelial CellsExtracellular MatrixFluorescent Antibody TechniqueGene Expression ProfilingGene OntologyHemodynamicsHumansIntegrin alpha6Integrin alpha ChainsIntegrin beta4Integrin beta ChainsIntegrinsIntegrin alpha6Integrin alpha ChainsIntegrin beta4Integrin beta ChainsIntegrinsITGA6 protein, humanITGB4 protein, humanLAMA4 protein, humanLamininTumor Necrosis Factor-alphabasement membraneendotheliumExtracellular matrixflowinflammationintegrinlabel-free quantificationlamininmass spectrometrySILAC

Identifiers

PMID32332107
PMCPMC7338090
OpenAlexW3020593866

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.