Evidence map›Paper›PMID 34360739›Full record

ReviewInternational journal of molecular sciences2021

Two Motors and One Spring: Hypothetic Roles of Non-Muscle Myosin II and Submembrane Actin-Based Cytoskeleton in Cell Volume Sensing.

Nadezhda Barvitenko, Muhammad Aslam, Alfons Lawen, Carlota Saldanha, Elisaveta Skverchinskaya, Giuseppe Uras, Alessia Manca, Antonella Pantaleo

Open access · goldAbstract readReview
In one paragraph

Review 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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 44% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. 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

8 authors at 6 institutions in 6 countries.

Nadezhda BarvitenkoIndependent Researcher, 191014 Saint-Petersburg, Russia.ORCID 0000-0002-9866-7545
Muhammad AslamDepartment of Internal Medicine I, Experimental Cardiology, Justus Liebig University, 35392 Giessen, Germany.ORCID 0000-0002-8529-4217
Alfons LawenDepartment of Biochemistry and Molecular Biology, School of Biomedical Sciences, Monash University, Clayton, VIC 3800, Australia.ORCID 0000-0001-6553-9945
Carlota SaldanhaInstitute of Biochemistry, Institute of Molecular Medicine, Faculty of Medicine University of Lisbon, 1649-028 Lisboa, Portugal.
Elisaveta SkverchinskayaSechenov Institute of Evolutionary Physiology and Biochemistry, 194223 St. Petersburg, Russia.ORCID 0000-0001-9587-6619
Giuseppe UrasDepartment of Clinical and Movement Neurosciences, Institute of Neurology, University College London, London NW3 2PF, UK.
Alessia MancaDepartment of Biomedical Science, University of Sassari, Viale San Pietro 43/B, 07100 Sassari, Italy.ORCID 0000-0001-7342-1023
Antonella PantaleoDepartment of Biomedical Science, University of Sassari, Viale San Pietro 43/B, 07100 Sassari, Italy.ORCID 0000-0003-2954-7053
University of Sassari · ITInstitute of Evolutionary Physiology and Biochemistry · RUJustus-Liebig-Universität Gießen · DEMonash University · AUUniversity College London · GBUniversity of Lisbon · PT

Funding

Univerity of Sassari NAUniversità degli Studi di Sassari NA
6 · The paper itself

Abstract

Changes in plasma membrane curvature and intracellular ionic strength are two key features of cell volume perturbations. In this hypothesis we present a model of the responsible molecular apparatus which is assembled of two molecular motors [non-muscle myosin II (NMMII) and protrusive actin polymerization], a spring [a complex between the plasma membrane (PM) and the submembrane actin-based cytoskeleton (smACSK) which behaves like a viscoelastic solid] and the associated signaling proteins. We hypothesize that this apparatus senses changes in both the plasma membrane curvature and the ionic strength and in turn activates signaling pathways responsible for regulatory volume increase (RVI) and regulatory volume decrease (RVD). During cell volume changes hydrostatic pressure (HP) changes drive alterations in the cell membrane curvature. HP difference has opposite directions in swelling versus shrinkage, thus allowing distinction between them. By analogy with actomyosin contractility that appears to sense stiffness of the extracellular matrix we propose that NMMII and actin polymerization can actively probe the transmembrane gradient in HP. Furthermore, NMMII and protein-protein interactions in the actin cortex are sensitive to ionic strength. Emerging data on direct binding to and regulating activities of transmembrane mechanosensors by NMMII and actin cortex provide routes for signal transduction from transmembrane mechanosensors to cell volume regulatory mechanisms.

Indexed as

Cell SizeSignal TransductionActin CytoskeletonActomyosinAnimalsCell MembraneHumansHydrostatic PressureMyosin Type IIActomyosinMyosin Type IIactin cortexactin polymerizationapoptosiscell volumemechanosensorsmigrationnon-muscle myosin IIproliferationshrinkageswelling

Identifiers

PMID34360739
PMCPMC8347689
OpenAlexW3184552784

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.