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Effect of ascorbic acid in vitro on lymphocyte reactivity to mitogens
The Journal of Nutrition
|November 1, 1980
Summary
High concentrations of ascorbic acid and dehydroascorbic acid inhibit human lymphocyte proliferation by affecting early metabolic processes. This immune cell response reduction occurred without impacting cell viability.
Area of Science:
- Immunology
- Cell Biology
- Biochemistry
Background:
- Ascorbic acid (vitamin C) is crucial for immune function.
- Its role in lymphocyte proliferation requires further elucidation, especially concerning its oxidized forms.
Purpose of the Study:
- To investigate the in vitro effects of ascorbic acid and dehydroascorbic acid on human lymphocyte proliferation.
- To determine the impact of these compounds on mitogen-stimulated immune responses.
Main Methods:
- Human lymphocytes were stimulated with phytohemagglutinin (PHA) and concanavalin A (Con A).
- Tritiated thymidine ([3H]TdR) incorporation was measured to assess proliferation.
- Cell viability, RNA, and protein synthesis were also evaluated.
Main Results:
- Physiologic and high concentrations of ascorbic acid and dehydroascorbic acid inhibited [3H]TdR incorporation in a dose-dependent manner.
- Inhibition occurred even when ascorbic acid was added late in the culture period.
- Non-cytotoxic concentrations of ascorbic acid and dehydroascorbic acid impaired lymphocyte activation.
Conclusions:
- Ascorbic acid and dehydroascorbic acid negatively regulate lymphocyte proliferation.
- These vitamins interfere with early metabolic events in mitogen-induced lymphocyte activation.
- The findings suggest a complex role for vitamin C in modulating immune cell responses.