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Phenotypic Tfh development promoted by CXCR5-controlled re-localization and IL-6 from radiation-resistant cells 被引量:3
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作者 Xin Chen Weiwei Ma +2 位作者 tingxin zhang LongyanWu Hai Qi 《Protein & Cell》 SCIE CAS CSCD 2015年第11期825-832,共8页
How follicular T-helper (Tfh) cells develop is incom- pletely understood. We find that, upon antigen exposure in vivo, both naive and antigen-experienced T cells sequentially upregulate CXCR5 and Bc16 within the fir... How follicular T-helper (Tfh) cells develop is incom- pletely understood. We find that, upon antigen exposure in vivo, both naive and antigen-experienced T cells sequentially upregulate CXCR5 and Bc16 within the first 24 h, relocate to the T-B border, and give rise to phenotypic Bcl6+CXCR5+ Tfh cells before the first cell division. CXCR5 upregulation is more dependent on ICOS costimulation than that of Bcl6, and early Bcl6 induction requires T-cell expression of CXCR5 and, presumably, relocation toward the follicle. This early and rapid upregulation of CXCR5 and Bcl6 depends on IL-6 produced by radiation-resistant cells. These results suggest that a Bcl6hiCXCR5hi phenotype does not automatically define a Tfh lineage but might reflect a state of antigen exposure and non-commitment to terminal effector fates and that niches in the T-B border and/or the follicle are important for optimal Bcl6 induction and maintenance. 展开更多
关键词 TFH CXCR5 BCL6 radiation-resistant cell IL-6
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