Phosphatidylcholine as a metabolic cue for determining B cell fate and function

磷脂酰胆碱作为决定B细胞命运和功能的代谢信号

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Abstract

In activated B cells, increased production of phosphatidylcholine (PtdCho), the most abundant cellular phospholipid, is handled primarily by the CDP-choline pathway. B cell-specific deletion of CTP:phosphocholine cytidylyltransferase α (CCTα), the rate-limiting enzyme in the CDP-choline pathway, led to augmented IgM secretion and reduced IgG production, suggesting that PtdCho synthesis is required for germinal center reactions. To specifically assess whether PtdCho influences B cell fate during germinal center responses, we examined immune responses in mice whereby PtdCho synthesis is disrupted in B cells that have undergone class switch recombination to IgG1 (referred to as either Cγ1(wt/wt), Cγ1(Cre/wt) or Cγ1(Cre/Cre) based on Cre copy number). Serum IgG1 was markedly reduced in naïve Cγ1(Cre/wt) and Cγ1(Cre/Cre) mice, while levels of IgM and other IgG subclasses were similar between Cγ1(Cre/wt) and Cγ1(wt/wt) control mice. Serum IgG2b titers were notably reduced and IgG3 titers were increased in Cγ1(Cre/Cre) mice compared with controls. Following immunization with T cell-dependent antigen NP-KLH, control mice generated high titer IgG anti-NP while IgG anti-NP titers were markedly reduced in both immunized Cγ1(Cre/wt) and Cγ1(Cre/Cre) mice. Correspondingly, the frequency of NP-specific IgG antibody-secreting cells was also reduced in spleens and bone marrow of Cγ1(Cre/wt) and Cγ. 1(Cre/Cre) mice compared to control mice. Interestingly, though antigen-specific IgM B cells were comparable between Cγ1(Cre/wt), Cγ1(Cre/Cre) and control mice, the frequency and number of IgG1 NP-specific B cells was reduced only in Cγ1(Cre/Cre) mice. These data indicate that PtdCho is required for the generation of both germinal center-derived B cells and antibody-secreting cells. Further, the reduction in class-switched ASC but not B cells in Cγ1(Cre/wt) mice suggests that ASC have a greater demand for PtdCho compared to germinal center B cells.

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