High dietary intake of vitamin C suppresses age-related thymic atrophy and contributes to maintenance of immune cells in vitamin C-deficient SMP30 knockout mice.
High dietary intake of vitamin C suppresses age-related thymic atrophy and contributes to maintenance of immune cells in vitamin C-deficient SMP30 knockout mice.
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饮食中摄入大量维生素 C 可抑制与年龄相关的胸腺萎缩,并有助于维持维生素 C 缺乏的 SMP30 基因敲除小鼠的免疫细胞。
DOI:
10.1017/s0007114514003857
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发表时间:
2015
期刊:
影响因子:
--
通讯作者:
A.
中科院分区:
文献类型:
--
作者:
Uchio;R.;Hirose;Y.;Murosaki;S.;Yamamoto;Y.;Ishigami;A.
Vitamin C (VC) is an essential nutrient for humans and certain other animals. It has antioxidant properties and has been reported to ameliorate oxidative damage to lipids, DNA and proteins. However, the effects of VC on immune function are poorly understood, especially the influence of long-term high-dose VC intake on the number and function of immune cells. In the present study, to evaluate the immune effects of VC, VC-deficient senescence marker protein-30 knockout (SMP30KO) mice were fed a diet containing the recommended level of VC (20 mg/kg per d; 0·02 % VC) or a high level of VC (200 mg/kg per d; 0·2 % VC) for 1 year. The plasma VC concentration of the 0·02 % group was the same as that of age-matched C57BL/6 mice after 1 year of feeding; however, plasma VC concentration and thymus weight were significantly higher in the 0·2 % VC group than in the 0·02 % VC group. The total counts of leucocytes, lymphocytes, granulocytes and monocytes in the peripheral blood, as well as the number of splenocytes and thymocytes, were all significantly higher in the 0·2 % VC group than in the 0·02 % VC group. In addition, the number of naive T cells in peripheral blood lymphocytes, the number of memory T-cell populations in splenocytes, and the number of cluster of differentiation (CD)4+CD8+ or CD4+CD8− or CD4−CD8+ T cells in thymocytes were all markedly higher in the 0·2 % VC group than in the 0·02 % VC group after 1 year of dietary treatment. These results suggest that a long-term high-dose intake of VC is effective in the maintenance of immune cells, partly through the suppression of age-related thymic involution in VC-deficient SMP30KO mice.