Encephalitozoon hellem Infection Promotes Monocytes Extravasation
Yishan Lu1,2, Guozhen An1,2, Xue Wang1,2
1Sate Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing 400715, China.
Abstract:
Background: Microsporidia are a group of obligated intracellular fungus pathogens. Monocytes and the derivative macrophages are among the most important players in host immunity. The invasion of microsporidia may significantly affect the monocytes maturation and extravasation processes. Methods: We utilized a previously established microsporidia infection murine model to investigate the influences of microsporidia Encephalitozoon hellem (E. hellem) infection on monocyte maturation, releasing into the circulation and extravasation to the inflammation site. Flow cytometry and qPCR analysis were used to compare the monocytes and derivative macrophages isolated from bone marrow, peripheral blood and tissues of E. hellem-infected and control mice. Results: The results showed that the pro-inflammatory group of CD11b+Ly-6C+ monocytes are promoted in E. hellem-infected mice. Interestingly, the percentage of Ly-6C+ monocytes from E. hellem-infected mice are significantly lower in peripheral blood while significantly higher in the inflamed small intestine, together with up-regulated ratio of F4/80 macrophage in small intestine as well. Conclusions: Our findings demonstrated that E. hellem infection leads to promoted monocytes maturation in bone marrow, up-regulation of extravasation from peripheral blood to inflammation site and maturation into macrophages. Our study is the first systematic analysis of monocytes maturation and trafficking during microsporidia infection, and will provide better understanding of the pathogen-host interactions.
Insights
Microsporidia infection promotes monocyte maturation in bone marrow and their migration to inflamed tissues. This leads to increased macrophage numbers at infection sites, impacting host immunity.
Area of Science:
- Immunology
- Infectious Diseases
- Cell Biology
Background:
- Microsporidia are obligate intracellular fungal pathogens.
- Monocytes and macrophages are crucial for host immune responses.
- Microsporidian infections can disrupt monocyte function and trafficking.
Purpose of the Study:
- To investigate the impact of *Encephalitozoon hellem* infection on monocyte maturation and trafficking.
- To analyze monocyte and macrophage dynamics in a murine model of microsporidiosis.
- To understand pathogen-host interactions at the cellular level.
Main Methods:
- Utilized a murine model infected with *Encephalitozoon hellem*.
- Employed flow cytometry and qPCR analysis.
- Compared monocytes and macrophages from bone marrow, peripheral blood, and inflamed tissues.
Main Results:
- Promoted maturation of pro-inflammatory CD11b+Ly-6C+ monocytes in bone marrow.
- Reduced Ly-6C+ monocyte percentage in peripheral blood but increased presence in inflamed small intestine.
- Elevated F4/80 macrophage ratio in the small intestine of infected mice.
Conclusions:
- *E. hellem* infection enhances monocyte maturation and bone marrow release.
- Facilitates increased monocyte extravasation to inflammatory sites and subsequent macrophage differentiation.
- Provides novel insights into monocyte behavior during microsporidian infections.
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