Evidence map›Paper›PMID 36417863›Full record

ArticleCell reports2022

Double knockin mice show NF-κB trajectories in immune signaling and aging.

Shah Md Toufiqur Rahman, Mohammad Aqdas, Erik W Martin, Francesco Tomassoni Ardori, Preeyaporn Songkiatisak, Kyu-Seon Oh, Stefan Uderhardt, Sangwon Yun, Quia C Claybourne, Ross A McDevitt and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2022. 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
2.9field-weighted citation impact, top 7% 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, 34 citations in OpenAlex.

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  8. Autonomous Oscillations of NF-κB.Advances in experimental medicine and biology · 2026
    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

14 authors at 2 institutions in 1 country.

Shah Md Toufiqur RahmanLaboratory of Molecular Biology and Immunology, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Mohammad AqdasLaboratory of Molecular Biology and Immunology, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Erik W MartinLaboratory of Molecular Biology and Immunology, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Francesco Tomassoni ArdoriMouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD 21702, USA.
Preeyaporn SongkiatisakLaboratory of Molecular Biology and Immunology, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Kyu-Seon OhLaboratory of Molecular Biology and Immunology, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Stefan UderhardtLaboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Sangwon YunSchool of Medicine, Yale University, New Haven, CT 06510, USA.
Quia C ClaybourneComparative Medicine Section, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Ross A McDevittComparative Medicine Section, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Valentina GrecoSchool of Medicine, Yale University, New Haven, CT 06510, USA.
Ronald N GermainLaboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Lino TessarolloMouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD 21702, USA.
Myong-Hee SungLaboratory of Molecular Biology and Immunology, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA. Electronic address: sungm@nih.gov.
National Institutes of Health · USYale University · US

Funding

Functional decoding of signaling dynamics in single immune cellsZIAAG000380 · NIA · NATIONAL INSTITUTE ON AGING · PI SUNG, MYONG-HEE · 2016 to 2025
$29.0M
Intramural NIH HHS Z99 AG999999Intramural NIH HHS ZIA AG000380
6 · The paper itself

Abstract

In vitro studies suggest that mapping the spatiotemporal complexity of nuclear factor κB (NF-κB) signaling is essential to understanding its function. The lack of tools to directly monitor NF-κB proteins in vivo has hindered such efforts. Here, we introduce reporter mice with the endogenous RelA (p65) or c-Rel labeled with distinct fluorescent proteins and a double knockin with both subunits labeled. Overcoming hurdles in simultaneous live-cell imaging of RelA and c-Rel, we show that quantitative features of signaling reflect the identity of activating ligands, differ between primary and immortalized cells, and shift toward c-Rel in microglia from aged brains. RelA:c-Rel heterodimer is unexpectedly depleted in the nuclei of stimulated cells. Trajectories of subunit co-expression in immune lineages reveal a reduction at key cell maturation stages. These results demonstrate the power of these reporters in gaining deeper insights into NF-κB biology, with the spectral complementarity of the labeled NF-κB proteins enabling diverse applications.

Indexed as

NF-kappa BSignal TransductionAgingAnimalsCell LineCell NucleusMiceNF-kappa BCP: Immunologyc-Relendogenous knockinfluorescence correlation spectroscopyfluorescent fusion reporter miceinflammatory signalingintravital imaginglive microscopyNF-κBRela

Identifiers

PMID36417863
PMCPMC9764224
OpenAlexW4309593294

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.