Evidence map›Paper›PMID 35344172›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2022

Quantifying Human Natural Killer Cell Migration by Imaging and Image Analysis.

Amera L Martinez, Michael J Shannon, Shira E Eisman, Everardo Hegewisch-Solloa, Aneeza N Asif, Tasneem A M Ebrahim, Emily M Mace

Abstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 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
–field-weighted citation impact
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.

  1. Review
  2. Article
  3. Article
  4. Article
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.

Amera L MartinezDepartment of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA.
Michael J ShannonDepartment of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA.
Shira E EismanDepartment of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA.
Everardo Hegewisch-SolloaDepartment of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA.
Aneeza N AsifDepartment of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA.
Tasneem A M EbrahimDepartment of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA.
Emily M MaceDepartment of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA. em3375@cumc.columbia.edu.

Funding

DEFINING THE ROLE OF CELL MIGRATION IN HUMAN NK CELL DIFFERENTIATIONR01AI137073 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MACE, EMILY MARGARET · 2018 to 2022
$2.0M
Contact-dependent determinants of human natural killer cell developmentF31AI164869 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HEGEWISCH SOLLOA, EVERARDO · 2021 to 2023
$120k
NIAID NIH HHS F31 AI164869NIAID NIH HHS R01 AI137073
6 · The paper itself

Abstract

Migration is an important function for natural killer cells. Cell motility has implications in development, tissue infiltration, and cytotoxicity, and measuring the properties of natural killer (NK) cell migration using in vitro assays can be highly informative. Many researchers have an interest in studying properties of NK cell migration in the context of genetic mutation, disease, or in specific tissues and microenvironments. Motility assays can also provide information on the localization of proteins during different phases of cell migration. These assays can be performed on different surfaces for migration or coupled with chemoattractants and/or target cells to test functional outcomes or characterize cell migration speeds and phenotypes. NK cells undergo migration during differentiation in tissue, and these conditions can be modeled by culturing NK cells on a confluent bed of stromal cells on glass and imaging cell migration. Alternatively, fibronectin- or ICAM-1-coated surfaces promote NK cell migration and can be used as substrates. Here, we will describe techniques for the experimental setup and analysis of NK cell motility assays by confocal microscopy or in-incubator imaging using commercially available systems. Finally, we describe open-source software for analyzing cell migration using manual tracking or automated approaches and discuss considerations for the implementation of each of these methods.

Indexed as

Killer Cells, NaturalStromal CellsCell Migration AssaysCell MovementHumansMicroscopy, ConfocalCell adhesionCell migrationCell motilityFibronectinNatural killer cellStroma

Identifiers

PMID35344172
PMCPMC9159076

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.