Bryl Ewa, Witkowski Jacek M
Department of Immunopathology, Medical University of Gdansk, Debinki 7, Gdansk 80-211, Poland.
Exp Gerontol. 2004 Apr;39(4):587-95. doi: 10.1016/j.exger.2003.10.029.
Decreased proliferation of CD4(+) lymphocytes of elderly people is at least in part due to lowered proportion of cells that are capable of dividing and producing viable progeny (effective precursors). We show that age-dependent reduction in effective precursor numbers depends on the one hand, extensive, activation-dependent apoptosis occurring from the very onset of stimulation and, on the other, the accumulation of non-dividing, regulatory (suppressor) CD4(lo)CD25(+)CD28(lo) T cells. In addition, analysis of changes in surface expression of activation-related antigens, including CD25, CD69, and PCNA in consecutive generations of dividing CD4(+) cells traced by carboxyfluorescein diacetate succinimidyl ester staining showed variable patterns of these changes that may relate to various aspect of impaired division of these cells in elderly.
老年人CD4(+)淋巴细胞增殖减少至少部分归因于能够分裂并产生有活力后代的细胞(有效前体)比例降低。我们发现,有效前体数量随年龄增长而减少一方面取决于从刺激开始就发生的广泛的、激活依赖性凋亡,另一方面取决于非分裂性调节(抑制)性CD4(lo)CD25(+)CD28(lo) T细胞的积累。此外,通过羧基荧光素二乙酸琥珀酰亚胺酯染色追踪连续几代分裂CD4(+)细胞中激活相关抗原(包括CD25、CD69和PCNA)表面表达的变化分析显示,这些变化模式各异,可能与老年人这些细胞分裂受损的各个方面有关。