Evidence map›Paper›PMID 35507242›Full record

ArticleBiomechanics and modeling in mechanobiology2022

The role of adhesive receptor patterns on cell transport in complex microvessels.

Daniel F Puleri, Amanda Randles

Open access · greenAbstract read
In one paragraph

Article in Biomechanics and modeling in mechanobiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 48% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Distributed Acceleration of Adhesive Dynamics Simulations.Proceedings of 2022 29th European MPI Users' Group Meeting (EuroMPI/USA'2022) : September 26-28, 2022, Chattanooga, TN. European MPI Users' Group Meeting (29th : 2022 : Chattanooga, Tenn.) · 2022
    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

2 authors at 1 institution in 1 country.

Daniel F PuleriDepartment of Biomedical Engineering, Duke University, Durham, NC, 27708, USA.
Amanda RandlesDepartment of Biomedical Engineering, Duke University, Durham, NC, 27708, USA. amanda.randles@duke.edu.ORCID http://orcid.org/0000-0001-6318-3885
Duke University · US

Funding

Training in Medical ImagingT32EB001040 · NIBIB · DUKE UNIVERSITY · PI NIGHTINGALE, KATHRYN RADABAUGH · 2003 to 2018
$4.4M
Toward coupled multiphysics models of hemodynamics on leadership systemsDP5OD019876 · OD · UNIVERSITY OF CALIF-LAWRNC LVRMR NAT LAB · PI RANDLES, AMANDA E · 2014 to 2018
$2.0M
Technology for efficient simulation of cancer cell transportU01CA253511 · NCI · DUKE UNIVERSITY · PI RANDLES, AMANDA E · 2020 to 2022
$1.1M
NCI NIH HHS U01 CA253511NIBIB NIH HHS T32 EB001040NIH HHS DP5 OD019876NIH HHS DP5OD019876NIH HHS U01CA253511
6 · The paper itself

Abstract

Cell transport is governed by the interaction of fluid dynamic forces and biochemical factors such as adhesion receptor expression and concentration. Although the effect of endothelial receptor density is well understood, it is not clear how the spacing and local spatial distribution of receptors affect cell adhesion in three-dimensional microvessels. To elucidate the effect of vessel shape on cell trajectory and the arrangement of endothelial receptors on cell adhesion, we employed a three-dimensional deformable cell model that incorporates microscale interactions between the cell and the endothelium. Computational cellular adhesion models are systematically altered to assess the influence of receptor spacing. We demonstrate that the patterns of receptors on the vessel walls are a key factor guiding cell movement. In straight microvessels, we show a relationship between cell velocity and the spatial distribution of adhesive endothelial receptors, with larger receptor patches producing lower translational velocities. The joint effect of the complex vessel topology seen in microvessel shapes such as curved and bifurcated vessels when compared to straight tubes is explored with results which showed the spatial distribution of receptors affecting cell trajectory. Our findings here represent demonstration of the previously undescribed relationship between receptor pattern and geometry that guides cellular movement in complex microenvironments.

Indexed as

AdhesivesMicrovesselsCell AdhesionEndotheliumErythrocytesAdhesivesCell adhesionDeformable cellsEndothelial receptor densityImmersed boundary methodLattice Boltzmann methodMicrovessel bifurcationMicrovessel shape

Identifiers

PMID35507242
PMCPMC10777541
OpenAlexW4225380855

What OpenQuestion holds

Textmetadata
LicenceTDM
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 OpenQuestion graph.