期刊
JOURNAL OF IMMUNOLOGY
卷 183, 期 11, 页码 6903-6912出版社
AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.0900324
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类别
资金
- U.S. Public Health Service [DE011390, ES01247]
- Hematology Training [NHLBI-T32HL007152]
- Training Program in Oral Sciences [T32-DE007202]
- Parker B. Francis Fellowship
Protective humoral immune responses critically depend on the optimal differentiation of B cells into Ab-secreting cells. Because of the important role of Abs in fighting infections and in successful vaccination, it is imperative to identify mediators that control B cell differentiation. Activation of B cells through TLR9 by CpG-DNA induces plasma cell differentiation and Ab production. Herein, we examined the role of the peroxisome proliferator-activated receptor (PPAR)gamma/RXR alpha pathway on human B cell differentiation. We demonstrated that activated B cells up-regulate their expression of PPAR gamma. We also show that nanomolar levels of natural (15-deoxy-Delta (12,14)-prostaglandin J(2)) or synthetic (rosiglitazone) PPAR gamma ligands enhanced B cell proliferation and significantly stimulated plasma cell differentiation and Ab production. Moreover, the addition of GW9662, a specific PPAR gamma antagonist, abolished these effects. Retinoid X receptor (RXR) is the binding partner for PPAR gamma and is required to produce an active transcriptional complex. The simultaneous addition of nanomolar concentrations of the RXR alpha ligand (9-cis-retinoic acid) and PPAR gamma ligands to CpG-activated B cells resulted in additive effects, on B cell proliferation, plasma cell differentiation, and Ab production. Furthermore, PPAR gamma ligands alone or combined with 9-cis-retinoic acid enhanced CpG-induced expression of Cox-2 and the plasma cell transcription factor BLIMP-1. Induction of these important regulators of B cell differentiation provides a possible mechanism for the B cell-enhancing effects of PPAR gamma ligands. These new findings indicate that low doses of PPAR gamma/RXP alpha ligands could be used as a new type of adjuvant to stimulate Ab production. The Journal of Immunology, 2009, 183: 6903-6912.
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