Evidence map›Paper›PMID 35318004›Full record

ArticleBiophysical journal2022

Distinct timing of neutrophil spreading and stiffening during phagocytosis.

Alexandra Zak, Sophie Dupré-Crochet, Elodie Hudik, Avin Babataheri, Abdul I Barakat, Oliver Nüsse, Julien Husson

Open access · greenAbstract read
In one paragraph

Article in Biophysical journal, 2022. 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
1.3field-weighted citation impact, top 25% 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, 11 citations in OpenAlex.

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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 at 1 institution in 1 country.

Alexandra ZakLadHyX, CNRS, École polytechnique, Institut Polytechnique de Paris, Palaiseau, France; Institut de Chimie Physique, CNRS UMR 8000, Université Paris-Saclay, Orsay, France.
Sophie Dupré-CrochetInstitut de Chimie Physique, CNRS UMR 8000, Université Paris-Saclay, Orsay, France.
Elodie HudikInstitut de Chimie Physique, CNRS UMR 8000, Université Paris-Saclay, Orsay, France.
Avin BabataheriLadHyX, CNRS, École polytechnique, Institut Polytechnique de Paris, Palaiseau, France.
Abdul I BarakatLadHyX, CNRS, École polytechnique, Institut Polytechnique de Paris, Palaiseau, France.
Oliver NüsseInstitut de Chimie Physique, CNRS UMR 8000, Université Paris-Saclay, Orsay, France.
Julien HussonLadHyX, CNRS, École polytechnique, Institut Polytechnique de Paris, Palaiseau, France. Electronic address: julien.husson@ladhyx.polytechnique.fr.
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phagocytic cells form the first line of defense in an organism, engulfing microbial pathogens. Phagocytosis involves cell mechanical changes that are not yet well understood. Understanding these mechanical modifications promises to shed light on the immune processes that trigger pathological complications. Previous studies showed that phagocytes undergo a sequence of spreading events around their target followed by an increase in cell tension. Seemingly in contradiction, other studies observed an increase in cell tension concomitant with membrane expansion. Even though phagocytes are viscoelastic, few studies have quantified viscous changes during phagocytosis. It is also unclear whether cell lines behave mechanically similarly to primary neutrophils. We addressed the question of simultaneous versus sequential spreading and mechanical changes during phagocytosis by using immunoglobulin-G-coated 8- and 20-μm-diameter beads as targets. We used a micropipette-based single-cell rheometer to monitor viscoelastic properties during phagocytosis by both neutrophil-like PLB cells and primary human neutrophils. We show that the faster expansion of PLB cells on larger beads is a geometrical effect reflecting a constant advancing speed of the phagocytic cup. Cells become stiffer on 20- than on 8-μm beads, and the relative timing of spreading and stiffening of PLB cells depends on target size: on larger beads, stiffening starts before maximal spreading area is reached but ends after reaching maximal area. On smaller beads, the stiffness begins to increase after cells have engulfed the bead. Similar to PLB cells, primary cells become stiffer on larger beads but start spreading and stiffen faster, and the stiffening begins before the end of spreading on both bead sizes. Our results show that mechanical changes in phagocytes are not a direct consequence of cell spreading and that models of phagocytosis should be amended to account for causes of cell stiffening other than membrane expansion.

Indexed as

NeutrophilsPhagocytosisCell LineCell MembraneHumansPhagocytes

Identifiers

PMID35318004
PMCPMC9072703
OpenAlexW4220749042

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.