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Updated: Feb 10, 2026

A Macrophage-Tumor Spheroid Co-Invasion Assay
Published on: January 24, 2025
Phenotyping Tumor-Associated Macrophages
1Division of Pulmonary and Critical Care Medicine, Department of Medicine, Duke University School of Medicine, Durham, NC, USA.
Insights
This study presents a flow cytometry method to analyze immune cells in tumor tissues. The approach enables detailed characterization of immune cell composition and function, including tumor-associated macrophages.
Area of Science:
- Immunology
- Cancer Biology
- Cellular Biology
Background:
- Tumor microenvironment research requires detailed immune cell analysis.
- Current methods for immune cell characterization in nonlymphoid tissues can be complex.
Purpose of the Study:
- To describe a standardized multi-parametric flow cytometry approach.
- To enable comprehensive immune cell profiling in tumor-bearing murine nonlymphoid tissues.
- To facilitate the phenotyping of tumor-associated macrophages.
Main Methods:
- Processing of nonlymphoid tissues from tumor-bearing mice.
- Utilizing a base antibody panel for broad immune cell identification.
- Single staining condition for simultaneous analysis of multiple immune cell types.
Main Results:
- Successful characterization of major immune cell types within nonlymphoid tissues.
- Demonstration of the panel's utility for phenotyping tumor-associated macrophages.
- Provides a foundation for examining immune cell composition, phenotype, and function.
Conclusions:
- The described flow cytometry approach offers an efficient method for immune cell analysis in tumor tissues.
- This technique aids in understanding the immune landscape of the tumor microenvironment.
- Facilitates deeper investigation into the role of specific immune cells, such as macrophages, in cancer.
Abstract:
Multi-parametric flow cytometry of tumor-bearing murine nonlymphoid tissue allows for characterization, isolation, and examination of immune cell composition, phenotype, and function. Here we describe an approach to process nonlymphoid tissues and then utilize a base antibody panel to define all of the major immune cell types in a single staining condition. This panel can be used to phenotype tumor-associated macrophages.
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