Abstract
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. JEM © The Rockefeller University Press.
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CITATION STYLE
Kuo, T. C., Shaffer, A. L., Haddad, J., Yong, S. C., Staudt, L. M., & Calame, K. (2007). Repression of BCL-6 is required for the formation of human memory B cells in vitro. Journal of Experimental Medicine, 204(4), 819–830. https://doi.org/10.1084/jem.20062104
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