Jönsson J I, Phillips R A
Department of Immunology, University of Toronto, Ontario, Canada.
Cell Immunol. 1993 Apr 1;147(2):267-78. doi: 10.1006/cimm.1993.1068.
Using short-term culture assays to quantify the activity of B220+ B cell progenitors from bone marrow of young and old mice, we observed a decrease with age in the ability of B220+ cells in bone marrow to proliferate in IL-7. Dose-response curves showed no difference between young and old mice in the amount of IL-7 required to stimulate B220+ cells. However, the B220+ cells from the bone marrow of old donors (> 20 weeks) contained two- to fivefold fewer cells responsive to IL-7 than the identical cell population isolated from young donors. Similar results were obtained with mice up to 48 weeks of age from three different strains, BALB/c, C57BL/6, and C.B-17. These data provide evidence for a small, but reproducible, age-associated decrease in B cell production.
通过短期培养分析来量化年轻和老年小鼠骨髓中B220+B细胞祖细胞的活性,我们观察到随着年龄增长,骨髓中B220+细胞在IL-7中增殖的能力下降。剂量反应曲线显示,刺激B220+细胞所需的IL-7量在年轻和老年小鼠之间没有差异。然而,来自老年供体(>20周)骨髓的B220+细胞对IL-7有反应的细胞数量比从年轻供体分离的相同细胞群体少两到五倍。从三种不同品系BALB/c、C57BL/6和C.B-17中选取的48周龄小鼠也得到了类似结果。这些数据为B细胞生成中与年龄相关的、虽小但可重复的减少提供了证据。