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Selenium and immune cell functions. I. Effect on lymphocyte proliferation and production of interleukin 1 and
L Kiremidjian-Schumacher1, M Roy, H I Wishe
1Department of Oral Medicine and Pathology, New York University Dental Center, New York 10010.
Insights
Dietary selenium (Se) impacts immune cell function. Selenium deficiency impaired lymphocyte proliferation, while supplementation enhanced it, suggesting mechanisms independent of interleukin-2 or interleukin-1.
Area of Science:
- Immunology
- Nutritional Science
- Cell Biology
Background:
- Dietary selenium (Se) plays a crucial role in biological processes.
- Understanding selenium's impact on immune function is vital for health.
- Specific effects on lymphocyte activity require further investigation.
Purpose of the Study:
- To investigate the immunologic competence of lymphocytes in mice fed varying selenium levels.
- To determine how selenium deficiency or supplementation affects lymphocyte proliferation and cytokine production.
- To elucidate the relationship between selenium, lymphocyte response, and key interleukins.
Main Methods:
- Mice (C57BL/6J) were fed diets with deficient (0.02 ppm), normal (0.20 ppm), or supplemented (2.00 ppm) selenium for 8 weeks.
- Lymphocyte proliferation was assessed using mixed lymphocyte reactions (allogeneic stimulation) and phytohemagglutinin (mitogen stimulation).
- Production of interleukin-2 (IL-2) by lymphocytes and interleukin-1 (IL-1) by macrophages was measured.
Main Results:
- Selenium deficiency significantly inhibited lymphocyte proliferation in response to both allogeneic and mitogenic stimuli.
- Selenium supplementation significantly enhanced lymphocyte proliferation compared to the control diet.
- Interleukin-2 and interleukin-1 production levels did not significantly differ between selenium-deficient, supplemented, and control groups.
Conclusions:
- Selenium status significantly modulates lymphocyte proliferative capacity.
- The observed effects of selenium on lymphocyte proliferation appear to be independent of IL-2 and IL-1 production levels.
- These findings highlight selenium's critical role in immune cell responsiveness.
Abstract:
The dietary intake of selenium (Se) has been shown to influence the development and expression of various biologic processes. This study examined the immunologic competence of lymphocytes from C57BL/6J mice maintained for 8 weeks on Se-deficient (0.02 ppm Se), normal (0.20 ppm Se, as sodium selenite), or Se-supplemented (2.00 ppm Se) Torula yeast-based diets. The ability of the cells to recognize alloantigens, to proliferate in response to stimuli, and to produce interleukin 2 (IL-2) was determined. Se deficiency significantly inhibited the ability of the lymphocytes to proliferate in response to allogeneic stimulation in the mixed lymphocyte reaction or to mitogen stimulation by phytohemagglutinin, whereas Se supplementation significantly enhanced both responses. In contrast, the amounts of IL-2 and interleukin 1 (IL-1) produced by lymphocytes and macrophages, respectively, removed from Se-deficient or Se-supplemented animals did not differ significantly from the amounts of IL-2 and IL-1 produced by cells removed from animals maintained on the control diet. These results suggest that the mechanism(s) responsible for the observed effects of Se on lymphocyte proliferation are independent of the levels of IL-2 or IL-1.
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