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.
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16 April 2007
Article|
April 02 2007
Repression of BCL-6 is required for the formation of human memory B cells in vitro
Tracy C. Kuo,
Tracy C. Kuo
1Department of Microbiology, Columbia University Medical Center, New York, NY 10032
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Arthur L. Shaffer,
Arthur L. Shaffer
2Metabolism Branch, Center for Cancer Research, National Cancer Institute Bethesda, MD 20892
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Joseph Haddad, Jr.,
Joseph Haddad, Jr.
3Division of Pediatric Otolaryngology, Columbia University Medical Center, New York, NY 10032
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Yong Sung Choi,
Yong Sung Choi
4Laboratory of Cellular Immunology, Ochsner Clinic Foundation, New Orleans, LA 70121
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Louis M. Staudt,
Louis M. Staudt
2Metabolism Branch, Center for Cancer Research, National Cancer Institute Bethesda, MD 20892
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Kathryn Calame
Kathryn Calame
1Department of Microbiology, Columbia University Medical Center, New York, NY 10032
5Department of Biochemistry and Molecular Biophysics, Columbia University Medical Center, New York, NY 10032
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Tracy C. Kuo
1Department of Microbiology, Columbia University Medical Center, New York, NY 10032
Arthur L. Shaffer
2Metabolism Branch, Center for Cancer Research, National Cancer Institute Bethesda, MD 20892
Joseph Haddad, Jr.
3Division of Pediatric Otolaryngology, Columbia University Medical Center, New York, NY 10032
Yong Sung Choi
4Laboratory of Cellular Immunology, Ochsner Clinic Foundation, New Orleans, LA 70121
Louis M. Staudt
2Metabolism Branch, Center for Cancer Research, National Cancer Institute Bethesda, MD 20892
Kathryn Calame
1Department of Microbiology, Columbia University Medical Center, New York, NY 10032
5Department of Biochemistry and Molecular Biophysics, Columbia University Medical Center, New York, NY 10032
CORRESPONDENCE Kathryn Calame: [email protected]
Abbreviations used: 7-AAD, 7-amino actinomycin D; AID, activation-induced cytidine deaminase; BCMA, B cell maturation antigen; BCR, B cell receptor; GC, germinal center.
Received:
October 02 2006
Accepted:
February 28 2007
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2007
J Exp Med (2007) 204 (4): 819–830.
Article history
Received:
October 02 2006
Accepted:
February 28 2007
Citation
Tracy C. Kuo, Arthur L. Shaffer, Joseph Haddad, Yong Sung Choi, Louis M. Staudt, Kathryn Calame; Repression of BCL-6 is required for the formation of human memory B cells in vitro . J Exp Med 16 April 2007; 204 (4): 819–830. doi: https://doi.org/10.1084/jem.20062104
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