Related Experiment Video
Updated: Mar 6, 2026

Isolation of Murine Peritoneal Macrophages to Carry Out Gene Expression Analysis Upon Toll-like Receptors Stimulation
Published on: April 29, 2015
Induction of different activated phenotypes of mouse peritoneal macrophages grown in different tissue culture media
Tomoya Kawakami1, Atsushi Koike1, Fumio Amano2
1Laboratory of Biodefense and Regulation, Osaka University of Pharmaceutical Sciences, 4-20-1 Nasahara, Takatsuki, Osaka, 569-1094, Japan.
Abstract:
The role of activated macrophages in the host defense against pathogens or tumor cells has been investigated extensively. Many researchers have been using various culture media in in vitro experiments using macrophages. We previously reported that J774.1/JA-4 macrophage-like cells showed great differences in their activated macrophage phenotypes, such as production of reactive oxygen, nitric oxide (NO) or cytokines depending on the culture medium used, either F-12 (Ham's F-12 nutrient mixture) or Dulbecco modified Eagle's medium (DMEM). To examine whether a difference in the culture medium would influence the functions of primary macrophages, we used BALB/c mouse peritoneal macrophages in this study. Among the activated macrophage phenotypes, the expression of inducible NO synthase in LPS- and/or IFN-γ-treated peritoneal macrophages showed the most remarkable differences between F-12 and DMEM; i.e., NO production by LPS- and/or IFN-γ-treated cells was far lower in DMEM than in F-12. Similar results were obtained with C57BL mouse peritoneal macrophages. Besides, dilution of F-12 medium with saline resulted in a slight decrease in NO production, whereas that of DMEM with saline resulted in a significant increase, suggesting the possibility that DMEM contained some inhibitory factor(s) for NO production. However, such a difference in NO production was not observed when macrophage-like cell lines were examined. These results suggest that phenotypes of primary macrophages could be changed significantly with respect to host inflammatory responses by the surrounding environment including nutritional factors and that these altered macrophage phenotypes might influence the biological host defense.
Insights
Culture medium significantly impacts primary macrophage function, affecting host defense. Dulbecco modified Eagle
Area of Science:
- Immunology
- Cell Biology
Background:
- Activated macrophages are crucial for host defense against pathogens and tumors.
- In vitro studies often use various culture media for macrophage experiments.
- Previous work showed J774.1/JA-4 cells exhibit different phenotypes based on culture medium (F-12 vs. DMEM).
Purpose of the Study:
- To investigate if culture medium differences influence primary macrophage functions.
- To compare the effects of F-12 and DMEM on primary macrophage phenotypes.
Main Methods:
- Used BALB/c mouse peritoneal macrophages.
- Treated macrophages with lipopolysaccharide (LPS) and/or interferon-gamma (IFN-γ).
- Assessed nitric oxide (NO) production and inducible NO synthase expression.
Main Results:
- Primary macrophages showed significant differences in NO production between F-12 and DMEM.
- NO production was notably lower in DMEM compared to F-12.
- Diluting DMEM with saline increased NO production, suggesting inhibitory factors in DMEM.
Conclusions:
- Primary macrophage phenotypes, crucial for host inflammatory responses, are significantly altered by the culture environment.
- Nutritional factors in culture media can influence macrophage function and potentially impact biological host defense.
More Related Videos
07:44Studying the Effects of Tumor-Secreted Paracrine Ligands on Macrophage Activation using Co-Culture with Permeable Membrane Supports
Published on: November 28, 2019
10:35Assessment of Antibody-based Drugs Effects on Murine Bone Marrow and Peritoneal Macrophage Activation
Published on: December 26, 2017