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Updated: Aug 16, 2026

Isolation of Mouse Peritoneal Cavity Cells
Published on: January 29, 2010
Separation of murine peritoneal macrophages using Percoll density gradients
1Laboratoire d'Immunologie (CP 615), Faculté de Médecine, Université Libre de Bruxelles, Belgium.
This study presents a Percoll density gradient method to separate heterogeneous mouse and rat peritoneal macrophages. The technique effectively isolates macrophage subpopulations based on their specific densities for research applications.
Area of Science:
- Immunology
- Cell Biology
- Biochemistry
Background:
- Peritoneal macrophages exhibit functional and morphological heterogeneity.
- Isolating specific macrophage subpopulations is crucial for understanding their roles.
Purpose of the Study:
- To develop and describe a reproducible method for isolating peritoneal macrophage subpopulations.
- To enable the study of distinct macrophage subsets based on density.
Main Methods:
- Utilized continuous Percoll density gradients for analytical determination of specific cell densities.
- Employed discontinuous Percoll density gradients for preparative isolation of macrophage subpopulations.
- Applied the method to both mouse and rat peritoneal macrophages.
Main Results:
- Successfully determined specific cell densities of peritoneal macrophages.
- Efficiently isolated distinct macrophage subpopulations using density gradient centrifugation.
- Validated the procedure for both murine and rat models.
Conclusions:
- The described Percoll density gradient centrifugation is an effective technique for isolating peritoneal macrophage subpopulations.
- This method facilitates the study of macrophage heterogeneity in immunological and cellular research.
- The procedure is robust and applicable across different rodent species.
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