Evidence map›Paper›PMID 20171970›Full record

ArticleJournal of immunological methods2010

Quantitative measurement of F-actin accumulation at the NK cell immunological synapse.

Pinaki P Banerjee, Jordan S Orange

Abstract read
In one paragraph

Article in Journal of immunological methods, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

20 citing papers in PubMed, 28 citations in OpenAlex.

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  12. Quantitative Imaging Approaches to Study the CAR Immunological Synapse.Molecular therapy : the journal of the American Society of Gene Therapy · 2017
    Review
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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

2 authors at 1 institution in 1 country.

Pinaki P BanerjeeThe Children's Hospital of Philadelphia Research Institute, 3615 Civic Center Blvd., Philadelphia, PA 19104, USA.
Jordan S Orange
Children's Hospital of Philadelphia · US

Funding

Directing Function at the Natural Killer Cell Secretory Immunological SynapseR01AI067946 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ORANGE, JORDAN SCOTT · 2007 to 2019
$4.8M
Directing Function at the Natural Killer Cell Secretory Immunological SynapseR37AI067946 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Jordan Scott Orange · 2024 to 2026
$1.5M
Survival Analysis Methods for Transplantation StudiesR01AI067943 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DABROWSKA, DOROTA M · 2007 to 2009
$710k
NIAID NIH HHS R01 AI-067943NIAID NIH HHS R01 AI067946NIAID NIH HHS R37 AI067946
6 · The paper itself

Abstract

NK cells are lymphocytes of the innate immune system that can kill target cells after activation signal-induced directional secretion of lytic granule contents. This process depends upon F-actin polymerization at the NK cell immunological synapse (NKIS), which is the dynamic organization of molecules at the interface between the NK cell and target cell. Although F-actin accumulation at the NKIS is easily visualized, the ability to quantify F-actin at the NKIS is required to understand how F-actin reorganization and accumulation enable NK cell function. Here, we demonstrate several novel algorithms for measuring the content of F-actin accumulated at the NKIS with special emphasis upon actin contributed by the NK cell. These algorithms do not rely upon overexpressing fluorescent proteins or preincubating cells with vital fluorescent dyes. Using models of the activating and inhibitory NKIS as well as NK cells expressing fluorescent protein--cell surface receptor fusion proteins, these algorithms were tested and were used to quantitatively demonstrate that F-actin accumulates at the activating, but not at the inhibitory NKIS. With these approaches, we have also established mathematical formulas that should prove valuable in the comprehensive quantitative evaluation of the NKIS and be more broadly applicable in the measurement of the accumulation of any fluorophore at an intercellular junction.

Indexed as

AlgorithmsModels, BiologicalActinsCells, CulturedFluorescent DyesHumansImmunological SynapsesKiller Cells, NaturalMicroscopy, Fluorescence, MultiphotonActinsFluorescent Dyes

Identifiers

PMID20171970
PMCPMC2854315
OpenAlexW1992529333

What OpenQuestion 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 OpenQuestion graph.