Mitochondrial reactive oxygen species suppress humoral immune response through reduction of CD19 expression in B cells in mice. Issue 2 (21st December 2016) - Ogura, Masato
Abstract : Mitochondrial c‐Src inactivation reduces SDHA phosphorylation at Tyr215, resulting in enhancement of metabolic ROS production and basal levels of oxidative stress. This enhanced ROS suppress B‐cell receptor signaling through reduction of CD19 expression, leading to suppression of Ig production in B cells from male mice, but not from female mice. Abstract : Reactive oxygen species (ROS) are implicated in the modulation of diverse processes including immune responses. To evaluate the effects of metabolic ROS produced by mitochondria on B‐cell function and development, we created transgenic (Tg) mice expressing a phosphorylation‐defective mutant of succinate dehydrogenase A in B cells (bSDHA Y215F ). Splenic B cells in male, but not female, bSDHA Y215F mice produced three times more ROS than those in the control mice, and had decreased production of IgM, IgG1, and IgG3, and affinity maturation of IgG1 against T‐cell‐dependent antigens. Following immunization, the male bSDHA Y215F mice further displayed suppressed germinal center (GC) formation, and proliferation of GC B cells. Signaling analysis revealed defects in the intrinsic BCR responses, such as activation of Lyn, Btk, and PLCγ2, thus resulting in reduced intracellular Ca 2+ mobilization. Notably, the expression levels of B‐cell co‐receptor CD19 and its interaction with Lyn after BCR ligation were significantly reduced in B cells from male bSDHA Y215F mice. These results suggest that mitochondrial ROS suppress humoral immune responses through reduction of CD19 expression and resultant BCR signaling in B cells. Therefore, B‐cell immunity may be more labile to oxidative stress in male mice than in female mice.