Evidence map›Paper›PMID 33652934›Full record

ArticleInternational journal of molecular sciences2021

On the Role of Curved Membrane Nanodomains, and Passive and Active Skeleton Forces in the Determination of Cell Shape and Membrane Budding.

Luka Mesarec, Mitja Drab, Samo Penič, Veronika Kralj-Iglič, Aleš Iglič

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
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  4. A minimal physical model for curvotaxis driven by curved protein complexes at the cell's leading edge.Proceedings of the National Academy of Sciences of the United States of America · 2024
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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

5 authors.

Luka MesarecFaculty of Electrical Engineering, University of Ljubljana, SI-1000 Ljubljana, Slovenia.ORCID 0000-0002-8134-5566
Mitja DrabFaculty of Electrical Engineering, University of Ljubljana, SI-1000 Ljubljana, Slovenia.ORCID 0000-0002-2481-7598
Samo PeničFaculty of Electrical Engineering, University of Ljubljana, SI-1000 Ljubljana, Slovenia.
Veronika Kralj-IgličFaculty of Health Sciences, University of Ljubljana, SI-1000 Ljubljana, Slovenia.
Aleš IgličFaculty of Electrical Engineering, University of Ljubljana, SI-1000 Ljubljana, Slovenia.

Funding

Horizon 2020 801338Javna Agencija za Raziskovalno Dejavnost RS J1-9162Javna Agencija za Raziskovalno Dejavnost RS J2-8166Javna Agencija za Raziskovalno Dejavnost RS P2-0232Javna Agencija za Raziskovalno Dejavnost RS P3-0388
6 · The paper itself

Abstract

Biological membranes are composed of isotropic and anisotropic curved nanodomains. Anisotropic membrane components, such as Bin/Amphiphysin/Rvs (BAR) superfamily protein domains, could trigger/facilitate the growth of membrane tubular protrusions, while isotropic curved nanodomains may induce undulated (necklace-like) membrane protrusions. We review the role of isotropic and anisotropic membrane nanodomains in stability of tubular and undulated membrane structures generated or stabilized by cyto- or membrane-skeleton. We also describe the theory of spontaneous self-assembly of isotropic curved membrane nanodomains and derive the critical concentration above which the spontaneous necklace-like membrane protrusion growth is favorable. We show that the actin cytoskeleton growth inside the vesicle or cell can change its equilibrium shape, induce higher degree of segregation of membrane nanodomains or even alter the average orientation angle of anisotropic nanodomains such as BAR domains. These effects may indicate whether the actin cytoskeleton role is only to stabilize membrane protrusions or to generate them by stretching the vesicle membrane. Furthermore, we demonstrate that by taking into account the in-plane orientational ordering of anisotropic membrane nanodomains, direct interactions between them and the extrinsic (deviatoric) curvature elasticity, it is possible to explain the experimentally observed stability of oblate (discocyte) shapes of red blood cells in a broad interval of cell reduced volume. Finally, we present results of numerical calculations and Monte-Carlo simulations which indicate that the active forces of membrane skeleton and cytoskeleton applied to plasma membrane may considerably influence cell shape and membrane budding.

Indexed as

Cell ShapeComputer SimulationCytoskeletonElasticityErythrocyte MembraneErythrocytesHumansMembrane MicrodomainsModels, BiologicalModels, MolecularMonte Carlo Methodactin filamentsactive forceanisotropic shape of moleculesBAR domainscell shapecytoskeletonmembrane buddingmembrane skeletonNMIIA motor domainsorientational ordering

Identifiers

PMID33652934
PMCPMC7956631

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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.