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http://dx.doi.org/10.5115/acb.2010.43.1.25

Vitamin C acts indirectly to modulate isotype switching in mouse B cells  

Woo, A-Mi (Department of Anatomy and Tumor Immunity Medical Research Center, Seoul National University College of Medicine)
Kim, Jin-Hee (Department of Anatomy and Tumor Immunity Medical Research Center, Seoul National University College of Medicine)
Jeong, Young-Joo (Department of Anatomy and Tumor Immunity Medical Research Center, Seoul National University College of Medicine)
Maeng, Hyung-Gun (Department of Anatomy and Tumor Immunity Medical Research Center, Seoul National University College of Medicine)
Lee, Yong-Taek (Department of Rehabilitation Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine)
Kang, Jae-Seung (Department of Anatomy and Tumor Immunity Medical Research Center, Seoul National University College of Medicine)
Lee, Wang-Jae (Department of Anatomy and Tumor Immunity Medical Research Center, Seoul National University College of Medicine)
Hwang, Young-Il (Department of Anatomy and Tumor Immunity Medical Research Center, Seoul National University College of Medicine)
Publication Information
Anatomy and Cell Biology / v.43, no.1, 2010 , pp. 25-35 More about this Journal
Abstract
Vitamin C, one of essential micronutrients, has been reported to modulate the humoral immune responses in some mammals. We investigated whether vitamin C might modulate this response in mice by directly affecting B cells. Splenic B cells were isolated and activated by CD40- and B cell receptor-ligation in vitro. Th e cells were cultured with a pretreatment of vitamin C from 0 to 1 mM of concentrations. Vitamin C slightly increased apoptosis of B cells dose-dependently and behaved as an antioxidant. We found that in vivo administration of vitamin C by intraperitoneal injection aff ected isotype switching as previously reported: the titer of antigen-specific IgG1 antibody was decreased, while that of IgG2a was unaffected. Somewhat different from those observed in vivo, in vitro exposure to vitamin C slightly decreased isotype switching to IgG1 and increased isotype switching to IgG2a. Pretreatment with vitamin C in the safe range did not affect either proliferation of cultured B cells or the expression of CD80 and CD86 in those cells. Taken together, in vivo results suggest that vitamin C acts to modulate isotype switching in the mouse. However, because of our in vitro results, we suggest that the modulation exerted by vitamin C in vivo is by indirectly affecting B cells, perhaps by directly influencing other immune cells such as dendritic cells.
Keywords
Vitamin C; antioxidant; reactive oxygen species; mouse B cell; isotype switching;
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