Evidence map›Paper›PMID 40176347›Full record

ArticleBiophysical journal2025

Mechanical adaptivity of red blood cell flickering to extrinsic membrane stiffening by the solid-like biosurfactant β-Aescin.

Lara H Moleiro, Diego Herráez-Aguilar, Guillermo Solís-Fernández, Niccolo Caselli, Carina Dargel, Verónica I Dodero, José M Bautista, Thomas Hellweg, Francisco Monroy

Abstract read
In one paragraph

Article in Biophysical journal, 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

9 authors.

Lara H MoleiroDepartment of Physical Chemistry, Complutense University of Madrid, Madrid, Spain; Translational Biophysics, Health Research Institute (imas12), Hospital 12 de Octubre, Madrid, Spain; Physikalische und Biophysikalische Chemie, Universität Bielefeld, Bielefeld, Germany. Electronic address: larherna@ucm.es.
Diego Herráez-AguilarFaculty of Experimental Sciences, Francisco de Vitoria University (UFV), Madrid, Spain.
Guillermo Solís-FernándezDepartment of Physical Chemistry, Complutense University of Madrid, Madrid, Spain; Translational Biophysics, Health Research Institute (imas12), Hospital 12 de Octubre, Madrid, Spain; Molecular Imaging and Photonics, Department of Chemistry, KU Leuven, Heverlee, Belgium.
Niccolo CaselliDepartment of Physical Chemistry, Complutense University of Madrid, Madrid, Spain; Translational Biophysics, Health Research Institute (imas12), Hospital 12 de Octubre, Madrid, Spain.
Carina DargelPhysikalische und Biophysikalische Chemie, Universität Bielefeld, Bielefeld, Germany.
Verónica I DoderoPhysikalische und Biophysikalische Chemie, Universität Bielefeld, Bielefeld, Germany.
José M BautistaDepartment of Biochemistry and Molecular Biology, Faculty of Veterinary, Complutense University of Madrid, Madrid, Spain; Translational Malaria Laboratory, Health Research Institute (imas12), Hospital 12 de Octubre, Madrid, Spain.
Thomas HellwegPhysikalische und Biophysikalische Chemie, Universität Bielefeld, Bielefeld, Germany. Electronic address: thomas.hellweg@uni-bielefeld.de.
Francisco MonroyDepartment of Physical Chemistry, Complutense University of Madrid, Madrid, Spain; Translational Biophysics, Health Research Institute (imas12), Hospital 12 de Octubre, Madrid, Spain. Electronic address: monroy@ucm.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

β-Aescin is a natural additive employed for treatments of vascular insufficiency, hence its impact in red blood cell (RBC) adaptivity has been conjectured. Here, we report a study about the mechanical impact of the membrane stiffener aescin on the flickering motions of live RBCs maintained at the homeostatic status. An active flickering, or nonequilibrium fluctuation dynamics has been revealed by mapping flickering motions in single RBCs treated or not with aescin. Experiments show that active RBC flickers adapt mechanically to β-escin, unlike the passive thermal fluctuations observed in lipid bilayers without an active skeleton. Mechanical connections for active flickering are theoretically argued to exist between an effective viscoelastic softness bestowed by the spectrin membrane cytoskeleton and the observed stiffness imposed by aescin as a rigidity modulator. From the unveiled diffusive mechanics, we model an adaptive RBC homeostasis that recapitulates the active flickering phenomenon as an optimal membrane softness upon a regulated friction as observed under aescin-induced membrane hardening. From a physiological perspective, RBC flicker adaptiveness to rigidization is discussed according to regulatory principles of energy conservation and minimal dissipation.

Indexed as

Adaptation, PhysiologicalErythrocyte MembraneErythrocytesEscinMechanical PhenomenaSurface-Active AgentsBiomechanical PhenomenaHumansEscinSurface-Active Agents

Identifiers

PMID40176347
PMCPMC12256860

What Socratic holds

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LicenceCC BY
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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 Socratic graph.