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Investigation of Macrophage Polarization Using Bone Marrow Derived Macrophages
Published on: June 23, 2013
INFLUENCE OF BIFIDOBACTERIUM ANIMALIS SUBSP. LACTIS BB-12 AND LACTOBACILLUS RHAMNOSUS GG ON POLARIZATION OF
N Fedosova1, T Symchych1, S Gogol1
1R.E. Kavetsky Institute of Experimental Pathology, Oncology and Radiobiology of the NAS of Ukraine, Kyiv, Ukraine.
Two probiotics, Bifidobacterium animalis subsp. lactis BB-12 (BB-12) and Lactobacillus rhamnosus GG (LGG), differentially impact tumor-associated macrophages (TAMs) in mice. LGG promotes M1 TAMs, while BB-12 induces M2 polarization, both retaining anti-tumor activity.
Area of Science:
- Immunology
- Microbiology
- Cancer Research
Background:
- The host immune system is significantly influenced by the gut microbiota.
- Microbiome effects are species, strain, and context-dependent.
- Tumor-associated macrophages (TAMs) play a critical role in cancer progression.
Purpose of the Study:
- To investigate the impact of Bifidobacterium animalis subsp. lactis BB-12 (BB-12) and Lactobacillus rhamnosus GG (LGG) on TAM polarization.
- To evaluate the functional consequences of probiotic-induced TAM polarization in a mouse model of Ehrlich carcinoma.
Main Methods:
- Female Balb/c mice with Ehrlich carcinoma were gavaged with BB-12, LGG, or saline.
- TAMs were isolated from tumor tissue on days 14, 21, and 28 post-tumor inoculation.
- Functional analyses included nitric oxide (NO) production, arginase activity, reactive oxygen species (ROS) production, and cytotoxic activity.
Main Results:
- LGG supplementation induced M1 TAM polarization, characterized by high NO and ROS production and cytotoxic activity.
- BB-12 supplementation resulted in M2 (potentially M2b) TAM polarization, with high arginase activity but preserved in vitro cytotoxic activity.
- Different probiotic strains elicited distinct TAM polarization states.
Conclusions:
- Probiotic consumption, specifically BB-12 and LGG, modulates TAM polarization in experimental tumors.
- Both BB-12 and LGG demonstrate potential in influencing the tumor microenvironment through TAM modulation.
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