B cells from young and old mice switch isotypes with equal frequencies after ex vivo stimulation

被引:9
|
作者
Knode, Lisa M. Russell [1 ]
Park, Han-Sol [1 ]
Maul, Robert W. [1 ]
Gearhart, Patricia J. [1 ]
机构
[1] NIA, Lab Mol Biol & Immunol, NIH, Baltimore, MD 21224 USA
基金
美国国家卫生研究院;
关键词
Age; Mice; B cell subsets; Ex vivo stimulation; Class switch recombination; Activation-induced deaminase; AGED MICE; DIVISION; DIFFERENTIATION; IMMUNOGLOBULIN; HYPERMUTATION; REFLECTS; DEFECTS; REPAIR; GENES; E47;
D O I
10.1016/j.cellimm.2019.103966
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To determine whether old B cells have the same capacity to switch isotypes as young cells, we purified splenic follicular, marginal zone, and age-associated B cell subsets from C57BL/6 mice. Cells were stimulated in culture with interleukin 4 and either lipopolysaccharide or anti-CD40, and switching to IgG1 was measured by flow cytometry of surface immunoglobulin. The results show that switching was robust in follicular and marginal zone B cells from old mice and was comparable to their young counterparts. However, age-associated B cells from old mice switched poorly relative to the other subsets. Expression of activation-induced deaminase, which initiates switching, was quantified by qPCR of mRNA, and it was equal between young and old follicular B cells. Thus, in this ex vivo system, the follicular and marginal zone cells from young and old mice behaved similarly, showing that the molecular machinery to perform switching is intact in old B cells.
引用
收藏
页数:3
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