Whitlock C A, Watson J D
J Exp Med. 1979 Dec 1;150(6):1483-97. doi: 10.1084/jem.150.6.1483.
The effect of age on the mitogenic and antigenic responsiveness of B cells is examined in spleen cell cultures of CBA/N and (CBA/N X DBA/2) F1 mice. Spleen cells from young male F1 mice (4- to 6-wk old) show lower mitogenic responses to lipopolysaccharide, a lower frequency of sheep erythrocytes (SRBC)-reactive B-cell precursors, and a lower percentage of Ig-bearing cells than age-matched female F1 mice. The expression of all three functions were found to increase with the age of the F1 male mice. Whereas male F1 mice at 60 wk of age showed an equivalent percentage of Ig-bearing spleen cells and a similar mitogenic responsiveness to LPS when compared to adult female F1 mice, the frequency of SRBC-reactive B-cell precursors remained threefold lower. These findings reveal that there is a slower maturation of B cells in mice expressing the X-linked defect and suggests that the defect has differential effects on the mechanisms of antigen and mitogen activation of B cells.
在CBA/N和(CBA/N×DBA/2)F1小鼠的脾细胞培养物中,研究了年龄对B细胞促有丝分裂和抗原反应性的影响。来自年轻雄性F1小鼠(4至6周龄)的脾细胞对脂多糖的促有丝分裂反应较低,对绵羊红细胞(SRBC)反应性B细胞前体的频率较低,且与年龄匹配的雌性F1小鼠相比,含Ig细胞的百分比更低。发现这三种功能的表达均随着F1雄性小鼠年龄的增长而增加。与成年雌性F1小鼠相比,60周龄的雄性F1小鼠含Ig脾细胞的百分比相当,对LPS的促有丝分裂反应相似,但SRBC反应性B细胞前体的频率仍低三倍。这些发现表明,表达X连锁缺陷的小鼠中B细胞成熟较慢,并表明该缺陷对B细胞抗原和丝裂原激活机制具有不同影响。