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.