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Age-related changes in mature CD4+ T cells:: cell cycle analysis
被引:10
作者:
Hale, TJ
Richardson, BC
Sweet, LI
McElligott, DL
Riggs, JE
Chu, EB
Glynn, JM
LaFrenz, D
Ernst, DN
Rochford, R
Hobbs, MV
机构:
[1] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Epidemiol, Ann Arbor, MI 48109 USA
[3] Rider Univ, Dept Biol, Lawrenceville, NJ 08648 USA
[4] PharMingen, San Diego, CA 92121 USA
[5] Harry S Truman Mem Vet Hosp, Dept Vet Affairs, Columbia, MO USA
关键词:
rodent;
T lymphocytes;
cell surface molecules;
cellular proliferation;
costimulation;
memory;
D O I:
10.1016/S0008-8749(03)00007-8
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
T cell proliferative responses decrease with age, but the mechanisms responsible are unknown. We examined the impact of age on memory and naive CD4(+) T cell entry and progression through the cell cycle using acridine orange to identify cell cycle stage. For both subsets, fewer stimulated cells from old donors were able to enter and progress through the first cell cycle, with an increased number of cells arrested in G(0) and fewer cells in post Go phases. The number of dead cells as assessed by sub-G(0) DNA was also significantly greater in the old group. CD4(+) T cells from old mice also exhibited a significant reduction in clonal history as assessed by CFSE staining. This was associated with a significant decline in cyclin D2 mRNA and protein. We propose that decreases in cyclin D2 are at least partially responsible for the proliferative decline found in aged CD4(+) T cells. (C) 2003 Elsevier Science (USA). All rights reserved.
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页码:51 / 62
页数:12
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