Evidence map›Paper›PMID 38322261›Full record

ArticleFrontiers in immunology2024

Evidence of collective influence in innate sensing using fluidic force microscopy.

Elizabeth J Mulder, Brittany Moser, Jennifer Delgado, Rachel C Steinhardt, Aaron P Esser-Kahn

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
1.0field-weighted citation impact, top 30% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 1 institution in 1 country.

Elizabeth J MulderEsser-Kahn Lab, Pritzker School of Molecular Engineering, University of Chicago, Chicago, IL, United States.
Brittany MoserEsser-Kahn Lab, Pritzker School of Molecular Engineering, University of Chicago, Chicago, IL, United States.
Jennifer DelgadoEsser-Kahn Lab, Pritzker School of Molecular Engineering, University of Chicago, Chicago, IL, United States.
Rachel C SteinhardtEsser-Kahn Lab, Pritzker School of Molecular Engineering, University of Chicago, Chicago, IL, United States.
Aaron P Esser-KahnEsser-Kahn Lab, Pritzker School of Molecular Engineering, University of Chicago, Chicago, IL, United States.
University of Chicago · US

Funding

ULTRASTRUCTURE AND CYTOMORPHOLOGY COREP30DK042086 · NIDDK · UNIVERSITY OF CHICAGO · PI PEKOW, JOEL · 1990 to 2025
$29.8M
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
Determining the Molecular Mechanism of Covalently Linked TLR AgonistsU01AI124286 · NIAID · UNIVERSITY OF CHICAGO · PI ESSER-KAHN, AARON P · 2016 to 2020
$3.2M
Probing short and long term consequences of Small and Large Bowel Microbiota Transplants on Host Physiology: Implications for the development of future live biotherapeuticsR01DK138072 · NIDDK · UNIVERSITY OF CHICAGO · PI EUGENE B CHANG, Kristina Brooke Martinez-Guryn · 2024 to 2026
$2.1M
NIAID NIH HHS 75N93019C00041NIAID NIH HHS U01 AI124286NIDDK NIH HHS P30 DK042086NIDDK NIH HHS R01 DK138072
6 · The paper itself

Abstract

The innate immune system initiates early response to infection by sensing molecular patterns of infection through pattern-recognition receptors (PRRs). Previous work on PRR stimulation of macrophages revealed significant heterogeneity in single cell responses, suggesting the importance of individual macrophage stimulation. Current methods either isolate individual macrophages or stimulate a whole culture and measure individual readouts. We probed single cell NF-κB responses to localized stimuli within a naïve culture with Fluidic Force Microscopy (FluidFM). Individual cells stimulated in naïve culture were more sensitive compared to individual cells in uniformly stimulated cultures. In cluster stimulation, NF-κB activation decreased with increased cell density or decreased stimulation time. Our results support the growing body of evidence for cell-to-cell communication in macrophage activation, and limit potential mechanisms. Such a mechanism might be manipulated to tune macrophage sensitivity, and the density-dependent modulation of sensitivity to PRR signals could have relevance to biological situations where macrophage density increases.

Indexed as

Immunity, InnateNF-kappa BMacrophagesMicroscopy, Atomic ForceReceptors, Pattern RecognitionNF-kappa BReceptors, Pattern RecognitionFluidFMfluidic force microscopyinnate immunitymacrophageNF-κBquorum licensingRAW 264.7resiquimod

Identifiers

PMID38322261
PMCPMC10844469
OpenAlexW4391143910

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.