Evidence map›Paper›PMID 29518073›Full record

ArticlePLoS computational biology2018

Method for the simulation of blood platelet shape and its evolution during activation.

Alexander E Moskalensky, Maxim A Yurkin, Artem R Muliukov, Alena L Litvinenko, Vyacheslav M Nekrasov, Andrei V Chernyshev, Valeri P Maltsev

Abstract read
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Article in PLoS computational biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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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

6 citing papers in PubMed.

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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

7 authors.

Alexander E MoskalenskyNovosibirsk State University, Novosibirsk, Russia.ORCID 0000-0002-9710-7757
Maxim A YurkinNovosibirsk State University, Novosibirsk, Russia.ORCID 0000-0002-3524-0093
Artem R MuliukovNovosibirsk State University, Novosibirsk, Russia.
Alena L LitvinenkoNovosibirsk State University, Novosibirsk, Russia.
Vyacheslav M NekrasovNovosibirsk State University, Novosibirsk, Russia.
Andrei V ChernyshevNovosibirsk State University, Novosibirsk, Russia.
Valeri P MaltsevNovosibirsk State University, Novosibirsk, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present a simple physically based quantitative model of blood platelet shape and its evolution during agonist-induced activation. The model is based on the consideration of two major cytoskeletal elements: the marginal band of microtubules and the submembrane cortex. Mathematically, we consider the problem of minimization of surface area constrained to confine the marginal band and a certain cellular volume. For resting platelets, the marginal band appears as a peripheral ring, allowing for the analytical solution of the minimization problem. Upon activation, the marginal band coils out of plane and forms 3D convoluted structure. We show that its shape is well approximated by an overcurved circle, a mathematical concept of closed curve with constant excessive curvature. Possible mechanisms leading to such marginal band coiling are discussed, resulting in simple parametric expression for the marginal band shape during platelet activation. The excessive curvature of marginal band is a convenient state variable which tracks the progress of activation. The cell surface is determined using numerical optimization. The shapes are strictly mathematically defined by only three parameters and show good agreement with literature data. They can be utilized in simulation of platelets interaction with different physical fields, e.g. for the description of hydrodynamic and mechanical properties of platelets, leading to better understanding of platelets margination and adhesion and thrombus formation in blood flow. It would also facilitate precise characterization of platelets in clinical diagnosis, where a novel optical model is needed for the correct solution of inverse light-scattering problem.

Indexed as

AlgorithmsBlood PlateletsCell ShapeComputational BiologyComputer SimulationHumansPlatelet Activation

Identifiers

PMID29518073
PMCPMC5860797

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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.