Evidence map›Paper›PMID 33205022›Full record

ArticleiScience2020

FcRγ Gene Editing Reprograms Conventional NK Cells to Display Key Features of Adaptive Human NK Cells.

Weiru Liu, Jeannine M Scott, Emma Langguth, Helena Chang, Peter H Park, Sungjin Kim

Open access · goldAbstract read
In one paragraph

Article in iScience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 41 citations in OpenAlex.

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  12. Nutrient transporter pattern in CD56Frontiers in immunology · 2024
    Article
  13. Article
  14. OMIP-098: A 26 parameter, 24 color flow cytometry panel for human memory NK cell phenotyping.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2023
    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 2 institutions in 1 country.

Weiru LiuCenter for Comparative Medicine, University of California, Davis, CA 95616, USA.
Jeannine M ScottDepartment of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI 48824, USA.
Emma LangguthCenter for Comparative Medicine, University of California, Davis, CA 95616, USA.
Helena ChangCenter for Comparative Medicine, University of California, Davis, CA 95616, USA.
Peter H ParkCenter for Comparative Medicine, University of California, Davis, CA 95616, USA.
Sungjin KimCenter for Comparative Medicine, University of California, Davis, CA 95616, USA.
University of California, Davis · USMichigan State University · US

Funding

FcRg-deficient human NK cells with protein Ab-dependent, anti-viral responsivenessR01AI110894 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KIM, SUNGJIN · 2015 to 2019
$2.0M
NIAID NIH HHS R01 AI110894
6 · The paper itself

Abstract

Adaptive human natural killer (NK) cells display significantly enhanced responsiveness to a broad-range of antibody-bound targets through the engagement of CD16 compared to conventional NK cells, yet direct reactivity against tumor targets is generally reduced. Adaptive NK cells also display a distinct phenotype and differential expression of numerous genes, including reduced expression of signaling adapter FcRγ and transcription factor PLZF. However, it is unclear whether differential expression of specific genes is responsible for the characteristics of adaptive NK cells. Using CRISPR-Cas9, we show deletion of FcRγ in conventional NK cells led to enhanced CD16 responsiveness, abolished cell surface expression of natural cytotoxicity receptors, NKp46 and NKp30, and dramatically reduced responsiveness to K562 and Raji tumor cells. However, deletion of PLZF had no notable effects. These results suggest multiple roles for FcRγ and identify its deficiency as an important factor responsible for the functional and phenotypic characteristics exhibited by adaptive NK cells.

Indexed as

CancerImmunologyMolecular Biology

Identifiers

PMID33205022
PMCPMC7649287
OpenAlexW3094432307

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.