Evidence map›Paper›PMID 26414320›Full record

ArticleJournal of molecular recognition : JMR2016

PeakForce Tapping resolves individual microvilli on living cells.

Hermann Schillers, Izhar Medalsy, Shuiqing Hu, Andrea L Slade, James E Shaw

Open access · hybridAbstract read
In one paragraph

Article in Journal of molecular recognition : JMR, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

39 citing papers in PubMed, 114 citations in OpenAlex.

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  12. 3D Generation of Multipurpose Atomic Force Microscopy Tips.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    Article
  13. Intranuclear HSV-1 DNA ejection induces major mechanical transformations suggesting mechanoprotection of nucleus integrity.Proceedings of the National Academy of Sciences of the United States of America · 2022
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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 2 institutions in 2 countries.

Hermann SchillersInstitute of Physiology II, University of Münster, Robert-Koch-Str. 27b, Münster, 48149, Germany.
Izhar MedalsyBruker Nano Surfaces Division, 112 Robin Hill Rd, Santa Barbara, CA, 93117, USA.
Shuiqing HuBruker Nano Surfaces Division, 112 Robin Hill Rd, Santa Barbara, CA, 93117, USA.
Andrea L SladeBruker Nano Surfaces Division, 112 Robin Hill Rd, Santa Barbara, CA, 93117, USA.
James E ShawBruker Nano Surfaces Division, 112 Robin Hill Rd, Santa Barbara, CA, 93117, USA.
Bruker (United States) · USUniversity of Münster · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microvilli are a common structure found on epithelial cells that increase the apical surface thus enhancing the transmembrane transport capacity and also serve as one of the cell's mechanosensors. These structures are composed of microfilaments and cytoplasm, covered by plasma membrane. Epithelial cell function is usually coupled to the density of microvilli and its individual size illustrated by diseases, in which microvilli degradation causes malabsorption and diarrhea. Atomic force microscopy (AFM) has been widely used to study the topography and morphology of living cells. Visualizing soft and flexible structures such as microvilli on the apical surface of a live cell has been very challenging because the native microvilli structures are displaced and deformed by the interaction with the probe. PeakForce Tapping® is an AFM imaging mode, which allows reducing tip-sample interactions in time (microseconds) and controlling force in the low pico-Newton range. Data acquisition of this mode was optimized by using a newly developed PeakForce QNM-Live Cell probe, having a short cantilever with a 17-µm-long tip that minimizes hydrodynamic effects between the cantilever and the sample surface. In this paper, we have demonstrated for the first time the visualization of the microvilli on living kidney cells with AFM using PeakForce Tapping. The structures observed display a force dependence representing either the whole microvilli or just the tips of the microvilli layer. Together, PeakForce Tapping allows force control in the low pico-Newton range and enables the visualization of very soft and flexible structures on living cells under physiological conditions.

Indexed as

AnimalsDogsEpithelial CellsImage Processing, Computer-AssistedKidneyMadin Darby Canine Kidney CellsMicroscopy, Atomic ForceMicrovilliAFMlive cell AFM probelow-force imagingMDCKPeakforce Tapping

Identifiers

PMID26414320
PMCPMC5054848
OpenAlexW2112272521

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.