Repression of BCL-6 is required for the formation of human memory B cells in vitro

被引:68
作者
Kuo, Tracy C.
Shaffer, Arthur L.
Haddad, Joseph, Jr.
Choi, Yong Sung
Staudt, Louis M.
Calame, Kathryn [1 ]
机构
[1] Columbia Univ, Med Ctr, Dept Microbiol, New York, NY 10032 USA
[2] NCI, Canc Res Ctr, Metab Branch, Bethesda, MD 20892 USA
[3] Columbia Univ, Med Ctr, Div Pediat Otolaryngol, New York, NY 10032 USA
[4] Alton Ochsner Med Fdn & Ochsner Clin, Cellular Immunol Lab, New Orleans, LA 70121 USA
[5] Columbia Univ, Med Ctr, Dept Biochem & Mol Biophys, New York, NY 10032 USA
关键词
D O I
10.1084/jem.20062104
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Memory B cells provide rapid protection to previously encountered antigens; however, how these cells develop from germinal center B cells is not well understood. A previously described in vitro culture system using human tonsillar germinal center B cells was used to study the transcriptional changes that occur during differentiation of human memory B cells. Kinetic studies monitoring the expression levels of several known late B cell transcription factors revealed that BCL-6 is not expressed in memory B cells generated in vitro, and gene expression profiling studies confirmed that BCL-6 is not expressed in these memory B cells. Furthermore, ectopic expression of BCL-6 in human B cell cultures resulted in formation of fewer memory B cells. In addition, the expression profile of in vitro memory B cells showed a unique pattern that includes expression of genes encoding multiple costimulatory molecules and cytokine receptors, antiapoptotic proteins, T cell chemokines, and transcription factors. These studies establish new molecular criteria for defining the memory B cell stage in human B cells.
引用
收藏
页码:819 / 830
页数:12
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