Iron deficiency reduces serum and in vitro secretion of interleukin-4 in mice independent of altered spleen cell proliferation

被引:35
作者
Kuvibidila, Solo R. [1 ,2 ,3 ]
Velez, Maria [1 ,2 ]
Gardner, Renee [1 ,2 ]
Penugonda, Kavitha [3 ]
Chandra, Lawrance C. [3 ]
Yu, Lolie [1 ,2 ]
机构
[1] Louisiana State Univ Hlth Sci Ctr, Res Inst Children, Dept Pediat, Div Res, New Orleans, LA 70118 USA
[2] Louisiana State Univ Hlth Sci Ctr, Div Hematol Oncol, Dept Pediat, New Orleans, LA 70118 USA
[3] Oklahoma State Univ, Dept Nutr Sci, Stillwater, OK 74078 USA
关键词
Cytokines; Interleukin-4; Iron deficiency; Mice; Thymus atrophy; INTERFERON-GAMMA; IGE SYNTHESIS; IL-4; PRODUCTION; T-CELLS; LYMPHOCYTE; SUBSETS; CD4(+); ACTIVATION; STRAINS; C57BL/6;
D O I
10.1016/j.nutres.2011.12.005
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 [营养与食品卫生学];
摘要
Iron deficiency, a worldwide public health problem in children and adult women, impairs innate and cell-mediated immunity including interferon-gamma secretion. Its effects on interleukin (IL)-4 have not been well investigated. Interleukin-4, a cytokine primarily secreted by TH2 lymphocytes, regulates B-cell proliferation and the switching of immunoglobulin (Ig)M to IgE subtypes; the latter is involved in the defense against helminth infection. Considering the fact that interferon-gamma is a potent inhibitor of IL-4, we hypothesize that iron deficiency would increase the secretion of IL-4 and IgE. We measured IL-4 in serum and supernatant of concanavalin A and anti-CD3 antibody-treated spleen cells from iron-deficient, control, pair-fed DBA and C57BL/6 mice (20-24/group) and iron-replete mice for 3, 7, and 14 days (8-13/group). Feeding the low-iron diet (5 ppm vs 50 ppm for the control diet) for 2 months significantly reduced the mean levels of hemoglobin, hematocrit, liver iron stores, thymus weight, and induced splenomegaly in both strains of mice (P <.001). Iron deficiency, and not pair-feeding, reduced plasma IL-4 levels (P < .05), although it did not significantly affect IgE levels. Iron deficiency, especially when associated with thymus atrophy, reduced in vitro IL-4 secretion by activated spleen cells, cell proliferation, and percentage of CD4(+)IL-4(+) cells (P < .05). Impaired cell proliferation did not fully explain reduced in vitro IL-4 secretion because iron-deficient mice with a normal thymus weight had a normal H-3-thymidine uptake but decreased supernatant IL-4. It was likely due to low percentage of CD4(+)IL-4(+). Iron repletion improved IL-4 measurements. Data suggest that iron deficiency has generalized negative effects on T-cell function. Unaltered plasma IgE may be due to other cytokines (ie, IL-13) that also modulate its secretion. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:107 / 115
页数:9
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