Evidence map›Paper›PMID 28445605›Full record

ArticleCytoskeleton (Hoboken, N.J.)2017

High-throughput cell mechanical phenotyping for label-free titration assays of cytoskeletal modifications.

Stefan Golfier, Philipp Rosendahl, Alexander Mietke, Maik Herbig, Jochen Guck, Oliver Otto

Open access · hybridAbstract read
In one paragraph

Article in Cytoskeleton (Hoboken, N.J.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 60 citations in OpenAlex.

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  19. Cardiomyocyte mechanodynamics under conditions of actin remodelling.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2019
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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

6 authors at 3 institutions in 1 country.

Stefan GolfierBiotechnology Center, Technische Universität Dresden, Dresden, Germany.
Philipp RosendahlBiotechnology Center, Technische Universität Dresden, Dresden, Germany.
Alexander MietkeMax-Planck-Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Maik HerbigBiotechnology Center, Technische Universität Dresden, Dresden, Germany.
Jochen GuckBiotechnology Center, Technische Universität Dresden, Dresden, Germany.
Oliver OttoBiotechnology Center, Technische Universität Dresden, Dresden, Germany.
TU Dresden · DEMax Planck Institute for Physics · DEMax Planck Institute for the Physics of Complex Systems · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mechanical fingerprint of cells is inherently linked to the structure of the cytoskeleton and can serve as a label-free marker for cell homeostasis or pathologic states. How cytoskeletal composition affects the physical response of cells to external loads has been intensively studied with a spectrum of techniques, yet quantitative and statistically powerful investigations in the form of titration assays are hampered by the low throughput of most available methods. In this study, we employ real-time deformability cytometry (RT-DC), a novel microfluidic tool to examine the effects of biochemically modified F-actin and microtubule stability and nuclear chromatin structure on cell deformation in a human leukemia cell line (HL60). The high throughput of our method facilitates extensive titration assays that allow for significance assessment of the observed effects and extraction of half-maximal concentrations for most of the applied reagents. We quantitatively show that integrity of the F-actin cortex and microtubule network dominate cell deformation on millisecond timescales probed with RT-DC. Drug-induced alterations in the nuclear chromatin structure were not found to consistently affect cell deformation. The sensitivity of the high-throughput cell mechanical measurements to the cytoskeletal modifications we present in this study opens up new possibilities for label-free dose-response assays of cytoskeletal modifications.

Indexed as

Staining and LabelingActinsBiomechanical PhenomenaChromatinComputer SystemsCytochalasin DCytoskeletonDepsipeptidesHigh-Throughput Screening AssaysHL-60 CellsHumansHydroxamic AcidsMicrotubulesNocodazolePaclitaxelPhenotypeActinsChromatinCytochalasin DDepsipeptidesHydroxamic AcidsjasplakinolideNocodazolePaclitaxeltrichostatin Acell mechanicscytoskeletonlabel-free cell characterizationreal-time deformability cytometry

Identifiers

PMID28445605
PMCPMC5601209
OpenAlexW2608402435

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.