Evidence map›Paper›PMID 31337806›Full record

ArticleScientific reports2019

A collagen-based microwell migration assay to study NK-target cell interactions.

Per E Olofsson, Ludwig Brandt, Klas E G Magnusson, Thomas Frisk, Joakim Jaldén, Björn Önfelt

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 32% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
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  5. Article
  6. Article
  7. Hydrogel Design to Understand and Guide 3D Cell Migration.Regenerative engineering and translational medicine · 2025
    Review
  8. Article
  9. Article
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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.

Per E OlofssonDivision of Biophysics, Department of Applied Physics, Science for Life Laboratory, KTH Royal Institute of Technology, Tomtebodavägen 23 A, 171 65, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-6019-8157
Ludwig BrandtDivision of Biophysics, Department of Applied Physics, Science for Life Laboratory, KTH Royal Institute of Technology, Tomtebodavägen 23 A, 171 65, Stockholm, Sweden.
Klas E G MagnussonDepartment of Signal Processing, ACCESS Linnaeus Centre, KTH Royal Institute of Technology, Stockholm, Sweden.
Thomas FriskDivision of Biophysics, Department of Applied Physics, Science for Life Laboratory, KTH Royal Institute of Technology, Tomtebodavägen 23 A, 171 65, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-3996-9279
Joakim JaldénDepartment of Signal Processing, ACCESS Linnaeus Centre, KTH Royal Institute of Technology, Stockholm, Sweden.ORCID http://orcid.org/0000-0001-6630-243X
Björn ÖnfeltDivision of Biophysics, Department of Applied Physics, Science for Life Laboratory, KTH Royal Institute of Technology, Tomtebodavägen 23 A, 171 65, Stockholm, Sweden. onfelt@kth.se.
Science for Life Laboratory · SEKTH Royal Institute of Technology · SEKarolinska Institutet · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer (NK) cell cytotoxicity in tissue is dependent on the ability of NK cells to migrate through the extracellular matrix (ECM) microenvironment. Traditional imaging studies of NK cell migration and cytotoxicity have utilized 2D surfaces, which do not properly reproduce the structural and mechanical cues that shape the migratory response of NK cells in vivo. Here, we have combined a microwell assay that allows long-term imaging and tracking of small, well-defined populations of NK cells with an interstitial ECM-like matrix. The assay allows for long-term imaging of NK-target cell interactions within a confined 3D volume. We found marked differences in motility between individual cells with a small fraction of the cells moving slowly and being confined to a small volume within the matrix, while other cells moved more freely. A majority of NK cells also exhibited transient variation in their motility, alternating between periods of migration arrest and movement. The assay could be used as a complement to in vivo imaging to study human NK cell heterogeneity in migration and cytotoxicity.

Indexed as

Cell CommunicationCell Migration Assays, LeukocyteCell MovementCollagenExtracellular MatrixHumansKiller Cells, NaturalTime-Lapse ImagingCollagen

Identifiers

PMID31337806
PMCPMC6650390
OpenAlexW2598361547

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.