Evidence map›Paper›PMID 26039164›Full record

ArticleBiophysical journal2015

Microfluidic study of enhanced deposition of sickle cells at acute corners.

Etienne Loiseau, Gladys Massiera, Simon Mendez, Patricia Aguilar Martinez, Manouk Abkarian

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 22 citations in OpenAlex.

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  8. Hypoxia-enhanced adhesion of red blood cells in microscale flow.Microcirculation (New York, N.Y. : 1994) · 2017
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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 at 4 institutions in 1 country.

Etienne LoiseauCentre National de la Recherche Scientifique UMR 5221, Laboratoire Charles Coulomb, Université de Montpellier, Montpellier, France.
Gladys MassieraCentre National de la Recherche Scientifique UMR 5221, Laboratoire Charles Coulomb, Université de Montpellier, Montpellier, France.
Simon MendezCentre National de la Recherche Scientifique UMR 5149, Institut de Mathématiques et de Modélisation de Montpellier, Université de Montpellier, Montpellier, France.
Patricia Aguilar MartinezFaculté de Médecine, Laboratoire d'Hématologie, Hôpital Saint Eloi, The Cardiovascular Health Research Unit de Montpellier, Montpellier, France.
Manouk AbkarianCentre National de la Recherche Scientifique UMR 5221, Laboratoire Charles Coulomb, Université de Montpellier, Montpellier, France; Centre National de la Recherche Scientifique UMR 5048-UM-Institut National de la Santé et de la Recherche Médicale UMR 1054, Centre de Biochimie Structurale, Montpellier, France. Electronic address: manouk.abkarian@univ-montp2.fr.
Centre National de la Recherche Scientifique · FRCentre de Biologie Structurale · FRInstitut Montpelliérain Alexander Grothendieck · FRUniversité de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sickle cell anemia is a blood disorder, known to affect the microcirculation and is characterized by painful vaso-occlusive crises in deep tissues. During the last three decades, many scenarios based on the enhanced adhesive properties of the membrane of sickle red blood cells have been proposed, all related to a final decrease in vessels lumen by cells accumulation on the vascular walls. Up to now, none of these scenarios considered the possible role played by the geometry of the flow on deposition. The question of the exact locations of occlusive events at the microcirculatory scale remains open. Here, using microfluidic devices where both geometry and oxygen levels can be controlled, we show that the flow of a suspension of sickle red blood cells around an acute corner of a triangular pillar or of a bifurcation, leads to the enhanced deposition and aggregation of cells. Thanks to our devices, we follow the growth of these aggregates in time and show that their length does not depend on oxygenation levels; instead, we find that their morphology changes dramatically to filamentous structures when using autologous plasma as a suspending fluid. We finally discuss the possible role played by such aggregates in vaso-occlusive events.

Indexed as

Microfluidic Analytical TechniquesAnemia, Sickle CellBlood PlateletsErythrocyte AggregationErythrocytesHemoglobinsHemolysisHumansLeukocytesOxygenHemoglobinsOxygen

Identifiers

PMID26039164
PMCPMC4457474
OpenAlexW1552281237

What OpenQuestion holds

Textmetadata
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.