Source:http://linkedlifedata.com/resource/pubmed/id/17056531
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2006-10-23
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pubmed:abstractText |
T cells are vulnerable to age-associated changes. Vitamin E has been shown to improve T cell functions in the old. We studied gene expression profiles of T cells to better understand the underlying mechanisms of age and vitamin E-induced changes in T cell function. Young and old C57BL mice were fed diets containing 30 (control) or 500 (supplemented) ppm of vitamin E for 4 wks. Gene expression profiles of T cells were assessed using microarray analysis with/without anti-CD3/anti-CD28 stimulation. Genes associated with cytokines/chemokines, transcriptional regulation, signal transduction, cell cycle, and apoptosis were significantly up-regulated upon stimulation. Higher SOCS3 and lower growth factor independent 1 (Gfi-1) expression in old T cells may contribute to age-associated decline in proliferation. Higher Gadd45 and lower Bcl2 expression may contribute to increased apoptosis in old T cells. Vitamin E supplementation resulted in higher expression of genes involved in cell cycle regulation (Ccnb2, Cdc2, Cdc6) in old T cells. Vitamin E supplementation resulted in higher up-regulation of IL-2 expression in young and old T cells and lower up-regulation of IL-4 expression in old T cells following stimulation. These findings suggest that aging has significant effects on the expression of genes associated with signal transduction, transcriptional regulation, and apoptosis pathways in T cells, and vitamin E has a significant impact on the expression of genes associated with cell cycle and Th1/Th2 balance in old T cells. Further studies are needed to determine whether these changes are due to the effects of aging at a single-cell level or to the shift in the ratio of naïve:memory T cells with age.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
177
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
6052-61
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pubmed:dateRevised |
2011-11-1
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pubmed:meshHeading |
pubmed-meshheading:17056531-Age Factors,
pubmed-meshheading:17056531-Aging,
pubmed-meshheading:17056531-Animals,
pubmed-meshheading:17056531-Apoptosis,
pubmed-meshheading:17056531-Cell Cycle,
pubmed-meshheading:17056531-Gene Expression,
pubmed-meshheading:17056531-Gene Expression Profiling,
pubmed-meshheading:17056531-Genes, Immunoglobulin,
pubmed-meshheading:17056531-Lymphocyte Activation,
pubmed-meshheading:17056531-Male,
pubmed-meshheading:17056531-Mice,
pubmed-meshheading:17056531-Mice, Inbred C57BL,
pubmed-meshheading:17056531-Receptors, Antigen, T-Cell,
pubmed-meshheading:17056531-T-Lymphocytes,
pubmed-meshheading:17056531-Vitamin E
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pubmed:year |
2006
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pubmed:articleTitle |
Age and vitamin E-induced changes in gene expression profiles of T cells.
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pubmed:affiliation |
Nutritional Immunology Laboratory, Jean Mayer U.S. Department of Agriculture Human Nutrition Research Center on Aging at Tufts University, 711 Washington Street, Boston, MA 02111, USA. sungnim.han@tufts.edu
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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