Monitoring Macrophage Polarization with Gene Expression Reporters and Bioluminescence Phasor Analysis

Macrophages exhibit a spectrum of behaviors upon activation and are generally classified as one of two types: inflammatory (M1) or anti-inflammatory (M2). Tracking these phenotypes in living cells can provide insight into immune function but remains a challenging pursuit. Existing methods are mostly limited to static readouts or are difficult to employ for multiplexed imaging in complex 3D environments while maintaining cellular resolution. We aimed to fill this void using bioluminescent technologies. Here we report genetically engineered luciferase reporters for the long-term monitoring of macrophage polarization via spectral phasor analysis. M1- and M2-specific promoters were used to drive the expression of bioluminescent enzymes in macrophage cell lines. The readouts were multiplexed and discernible in both 2D and 3D formats with single-cell resolution in living samples. Collectively, this work expands the toolbox of methods for monitoring macrophage polarization and provides a blueprint for monitoring other multifaceted networks in heterogeneous environments.

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Publication Details

Journal
Chemical & Biomedical Imaging
Published
2024-10-03
DOI
https://doi.org/10.1021/cbmi.4c00049
Citations
6
Primary Topic
bioluminescence and chemiluminescence research
Type
article
Field-Weighted Citation Impact
1.40

Funders

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article

Monitoring Macrophage Polarization with Gene Expression Reporters and Bioluminescence Phasor Analysis

Tanvi K. Sondhi, Jennifer A. Prescher, Michelle A. Digman, G Tedeschi et al.
6 citations
Chemical & Biomedical Imaging
bioluminescence and chemiluminescence research
1.40
article

Monitoring Macrophage Polarization with Gene Expression Reporters and Bioluminescence Phasor Analysis

Tanvi K. Sondhi, Jennifer A. Prescher, Michelle A. Digman, G Tedeschi, Lorenzo Scipioni, Mariana X. Navarro
article en
6 citations

Abstract

Macrophages exhibit a spectrum of behaviors upon activation and are generally classified as one of two types: inflammatory (M1) or anti-inflammatory (M2). Tracking these phenotypes in living cells can provide insight into immune function but remains a challenging pursuit. Existing methods are mostly limited to static readouts or are difficult to employ for multiplexed imaging in complex 3D environments while maintaining cellular resolution. We aimed to fill this void using bioluminescent technologies. Here we report genetically engineered luciferase reporters for the long-term monitoring of macrophage polarization via spectral phasor analysis. M1- and M2-specific promoters were used to drive the expression of bioluminescent enzymes in macrophage cell lines. The readouts were multiplexed and discernible in both 2D and 3D formats with single-cell resolution in living samples. Collectively, this work expands the toolbox of methods for monitoring macrophage polarization and provides a blueprint for monitoring other multifaceted networks in heterogeneous environments.

Chemical & Biomedical ImagingVol. 2(11)
Fluor (United States) (US), University of California, Irvine (US)
Paul G. Allen Frontiers Group, University of California, Irvine, National Institute of General Medical Sciences, Division of Graduate Education
Zero hunger
Openalex Percentile: Top 19%
bioluminescence and chemiluminescence research
1.40
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Monitoring Macrophage Polarization with Gene Expression Reporters and Bioluminescence Phasor Analysis — Tanvi K. Sondhi, Jennifer A. Prescher, et al. · Chemical & Biomedical Imaging (2024) | TGRS Research Map | TGRS