Evidence map›Paper›PMID 35977475›Full record

ArticleCell reports2022

NF-κB memory coordinates transcriptional responses to dynamic inflammatory stimuli.

Andrew G Wang, Minjun Son, Emma Kenna, Nicholas Thom, Savaş Tay

Abstract 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 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Commensal skin bacteria interact with the innate immune system to promote tail regeneration in Xenopus laevis tadpoles.Developmental dynamics : an official publication of the American Association of Anatomists · 2026
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  13. Single-nucleus proteomics identifies regulators of protein transport.bioRxiv : the preprint server for biology · 2024
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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

5 authors.

Andrew G WangPritzker School of Molecular Engineering, University of Chicago, Chicago, IL 60637, USA; Medical Scientist Training Program, University of Chicago, Chicago, IL 60637, USA.
Minjun SonPritzker School of Molecular Engineering, University of Chicago, Chicago, IL 60637, USA.
Emma KennaPritzker School of Molecular Engineering, University of Chicago, Chicago, IL 60637, USA.
Nicholas ThomPritzker School of Molecular Engineering, University of Chicago, Chicago, IL 60637, USA.
Savaş TayPritzker School of Molecular Engineering, University of Chicago, Chicago, IL 60637, USA. Electronic address: tays@uchicago.edu.

Funding

MEDICAL SCIENTIST TRAININGT32GM007281 · NIGMS · UNIVERSITY OF CHICAGO · PI CLARK, MARCUS RAMSAY · 1985 to 2022
$32.1M
Discovery of adjuvants via novel modulation of innate immune pathways for vaccines against influenza75N93019C00041 · NIAID · UNIVERSITY OF CHICAGO · PI ESSER-KAHN, AARON · 2019 to 2024
$10.0M
Medical Scientist National Research Service AwardT32GM150375 · NIGMS · UNIVERSITY OF CHICAGO · PI Raghavendra G Mirmira · 2023 to 2026
$5.5M
Understanding Mechanisms of Robust Information Processing by NF-kappaBR01GM128042 · NIGMS · UNIVERSITY OF CHICAGO · PI TAY, SAVAS · 2018 to 2022
$1.8M
NIAID NIH HHS 75N93019C00041NIGMS NIH HHS R01 GM128042NIGMS NIH HHS T32 GM007281NIGMS NIH HHS T32 GM150375
6 · The paper itself

Abstract

Many scenarios in cellular communication require cells to interpret multiple dynamic signals. It is unclear how exposure to inflammatory stimuli alters transcriptional responses to subsequent stimulus. Using high-throughput microfluidic live-cell analysis, we systematically profile the NF-κB response to different signal sequences in single cells. We find that NF-κB dynamics store the short-term history of received signals: depending on the prior pathogenic or cytokine signal, the NF-κB response to subsequent stimuli varies from no response to full activation. Using information theory, we reveal that these stimulus-dependent changes in the NF-κB response encode and reflect information about the identity and dose of the prior stimulus. Small-molecule inhibition, computational modeling, and gene expression profiling show that this encoding is driven by stimulus-dependent engagement of negative feedback modules. These results provide a model for how signal transduction networks process sequences of inflammatory stimuli to coordinate cellular responses in complex dynamic environments.

Indexed as

NF-kappa BSignal TransductionComputer SimulationCytokinesGene Expression ProfilingCytokinesNF-kappa Bcellular memoryCP: Immunologyinflammationinformation theoryinnate immune signalinglive-cell imagingmathematical modelingmicrofluidicsNF-κBpathogen-associated molecular patternssignaling dynamics

Identifiers

PMID35977475
PMCPMC10794069

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.