Evidence map›Paper›PMID 40402207›Full record

ArticlePflugers Archiv : European journal of physiology2025

SECS, drugs, and Rac1&Rho: regulation of EnNaC in vascular endothelial cells.

Benedikt Fels, Felix Fischer, Lisbeth Herrnboeck, David Beckers, Leon Niedzielski, Paul Roche, Alexandra Straeter, Ioana Alesutan, Johanna-Theres Borutta, Frederic Jaisser and 3 more

Abstract read
In one paragraph

Article in Pflugers Archiv : European journal of physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

13 authors.

Benedikt FelsInstitute of Physiology, University of Lübeck, Ratzeburger Str. 160, 23562, Lübeck, Germany.
Felix FischerInstitute of Physiology II, University of Münster, Münster, Germany.
Lisbeth HerrnboeckInstitute of Physiology II, University of Münster, Münster, Germany.
David BeckersInstitute of Physiology II, University of Münster, Münster, Germany.
Leon NiedzielskiInstitute of Physiology II, University of Münster, Münster, Germany.
Paul RocheInstitute of Physiology II, University of Münster, Münster, Germany.
Alexandra StraeterInstitute of Physiology II, University of Münster, Münster, Germany.
Ioana AlesutanInstitute for Physiology and Pathophysiology, Johannes Kepler University Linz, Linz, Austria.
Johanna-Theres BoruttaInstitute of Physiology, University of Lübeck, Ratzeburger Str. 160, 23562, Lübeck, Germany.
Frederic JaisserINSERM, UMRS 1166, ICAN, Sorbonne Université, Paris, France.
Olivier StaubDepartment of Biomedical Sciences, University of Lausanne, Lausanne, Switzerland.
Jakob VoelklInstitute for Physiology and Pathophysiology, Johannes Kepler University Linz, Linz, Austria.
Kristina Kusche-VihrogInstitute of Physiology, University of Lübeck, Ratzeburger Str. 160, 23562, Lübeck, Germany. kristina.kuschevihrog@uni-luebeck.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The endothelial ENaC (EnNaC) is mainly responsible for maintaining the mechanical properties of the endothelial cell surface, the sensitivity to the shear forces of the streaming blood and thus for vascular function. The correlation between EnNaC surface expression, the dynamics of the actin cortex, the mechanical stiffness, and nitric oxide release indicates a close structure-function relationship. Mechanical flexibility of the endothelial surface has been associated with proper vascular function, while chronic stiffening leads to endothelial dysfunction and the so-called 'stiff endothelial cell syndrome' (SECS). With the help of atomic force microscopy (AFM)-based nanoindentation and immunofluorescence staining in vitro and ex vivo, we investigated the underlying cellular mechanisms and signalling pathways of EnNaC-dependent endothelial behaviour. We were able to show that the interaction between EnNaC and the cortical cytoskeleton is mediated by the small GTPases RhoA, Rac1, and the Arp2/3 complex. The functional inhibition of EnNaC by the drugs amiloride and benzamil led to membrane removal of the channel within minutes. Furthermore, we could observe an involvement of mineralocorticoid receptor, SGK1 and Nedd4-2 in regulation of endothelial cell stiffness. Our study contributes further insights on complex regulation of EnNaC and elucidates its interaction with the actin cytoskeleton, which could be central to its role as a key regulator of vascular function in health and disease.

Indexed as

Endothelial CellsEpithelial Sodium Channelsrac1 GTP-Binding ProteinrhoA GTP-Binding ProteinActin-Related Protein 2-3 ComplexAmilorideAnimalsCells, CulturedHumansHuman Umbilical Vein Endothelial CellsImmediate-Early ProteinsProtein Serine-Threonine KinasesSerum-Glucocorticoid Regulated KinasesSignal TransductionActin-Related Protein 2-3 ComplexAmilorideEpithelial Sodium ChannelsImmediate-Early ProteinsProtein Serine-Threonine Kinasesrac1 GTP-Binding ProteinrhoA GTP-Binding ProteinSerum-Glucocorticoid Regulated KinasesAFMEndothelial nanomechanicsEnNaCNon-genomic aldosterone effects

Identifiers

PMID40402207
PMCPMC12152027

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Registered trials

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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.