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Are Actinomyces viscosus antigens B cell mitogens?
Journal of Immunology (Baltimore, Md. : 1950)
|April 1, 1977
Summary
Extracellular heteroglycan (ECHG) and sonicated cell supernatant (SCS) from Actinomyces viscosus stimulate lymphocyte proliferation. These compounds exhibit B cell mitogenicity, influencing immune responses.
Area of Science:
- Immunology
- Microbiology
- Biochemistry
Background:
- Actinomyces viscosus is a bacterium known to interact with the host immune system.
- Understanding microbial components that modulate lymphocyte activity is crucial for immunology.
Purpose of the Study:
- To investigate the mitogenic potential of Actinomyces viscosus extracellular heteroglycan (ECHG) and sonicated cell supernatant (SCS).
- To determine the specific lymphocyte populations targeted by these microbial components.
Main Methods:
- Lymphocyte proliferation assays using spleen and thoracic duct cells from germfree rats.
- Testing with spleen cells from conventional "nude" mice to assess T-cell independence.
- Analysis of B cell activation via plaque-forming cell assays against TNP-SRBC.
- Investigating the effect of alkaline hydrolysis on the mitogenic properties of ECHG.
Main Results:
- Both ECHG and SCS induced significant lymphocyte proliferation in rat cells.
- ECHG's mitogenicity was reduced after alkaline hydrolysis in rat lymphocytes but abolished in nude mouse lymphocytes.
- Spleen cells from rats produced plaque-forming cells against TNP-SRBC, indicating B cell activation.
- The results suggest that the mitogenic effects are primarily on B cells.
Conclusions:
- Actinomyces viscosus ECHG and SCS possess potent B cell mitogenicity.
- The structural integrity of ECHG is important for its mitogenic activity on B cells.
- These findings contribute to understanding bacterial modulation of the host immune system, specifically B cell responses.