机构:Tufts Univ, Jean Mayer USDA, Human Nutr Res Ctr, Nutr Immunol Lab, Boston, MA 02111 USA
Han, SN
Adolfsson, O
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Adolfsson, O
Lee, CK
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Lee, CK
Prolla, TA
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Prolla, TA
Ordovas, J
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Ordovas, J
Meydani, SN
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Meydani, SN
机构:
[1] Tufts Univ, Jean Mayer USDA, Human Nutr Res Ctr, Nutr Immunol Lab, Boston, MA 02111 USA
[2] Univ Wisconsin, Dept Genet & Med Genet, Madison, WI USA
[3] Tufts Univ, Jean Mayer USDA, Human Nutr Res Ctr, Nutr & Genom Lab, Boston, MA 02111 USA
来源:
VITAMIN E AND HEALTH
|
2004年
/
1031卷
关键词:
vitamin E;
gene expression;
immune cells;
aging;
D O I:
10.1196/annals.1331.010
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Aging is associated with dysregulation of immune cells, particularly T cells. Previous studies indicated that vitamin E improves T cell function, in part by a direct effect on T cells. We studied gene expression profile of T cells to better understand the underlying mechanisms of aging- and vitamin E-induced changes in T cell function. Young and old C57BL mice were fed diets containing 30 (control) or 500 (E) ppm of vitamin E for 4 weeks. T cells were purified from splenocytes by negative selection using magnetic beads (anti-Mac-1 and anti-MHC class II), then cultured with media or stimulated with anti-CD3 and anti-CD28. Gene expression profile was assessed using microarray analysis. Genes showing more than two-fold changes, P < 0.05 by ANOVA, and with at least one present call were selected. Aging had significant effects on genes involved in signal transduction, transcriptional regulation, and apoptosis pathways in T cells, while vitamin E had a significant effect on genes associated with the regulation of cell cycle.