Published January 23, 2024 | Version v1
Journal article Open

Evidence of collective influence in innate sensing using fluidic force microscopy

Description

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.

Data availability

The original contributions presented in the study are included in the article/Supplementary Materials. Further inquiries can be directed to the corresponding author. All data and code for this manuscript can be found at Mendeley Data, DOI: 10.17632/mfyddz6n8k.3.

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Additional details

Identifiers

DOI
10.3389/fimmu.2024.1340384
Other
oai:uchicago.tind.io:10744

Funding

National Institute for Allergy and Infectious Disease
75N93019C00041
National Institute for Allergy and Infectious Disease
5U01AI124286-06
Defense Threat Reduction Agency
HDTRA11810052
National Science Foundation
OMA-2121044
PEW Charitable Trusts
PEW Scholars
Camille Dreyfus Teacher Scholar Award

UChicago Information

Division(s)
Pritzker School of Molecular Engineering