| Literature DB >> 12150891 |
A L Shaffer1, Kuo I Lin, Tracy C Kuo, Xin Yu, Elaine M Hurt, Andreas Rosenwald, Jena M Giltnane, Liming Yang, Hong Zhao, Kathryn Calame, Louis M Staudt.
Abstract
Blimp-1, a transcriptional repressor, drives the terminal differentiation of B cells to plasma cells. Using DNA microarrays, we found that introduction of Blimp-1 into B cells blocked expression of a remarkably large set of genes, while a much smaller number was induced. Blimp-1 initiated this cascade of gene expression changes by directly repressing genes encoding several transcription factors, including Spi-B and Id3, that regulate signaling by the B cell receptor. Blimp-1 also inhibited immunoglobulin class switching by blocking expression of AID, Ku70, Ku86, DNA-PKcs, and STAT6. These findings suggest that Blimp-1 promotes plasmacytic differentiation by extinguishing gene expression important for B cell receptor signaling, germinal center B cell function, and proliferation while allowing expression of important plasma cell genes such as XBP-1.Entities:
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Year: 2002 PMID: 12150891 DOI: 10.1016/s1074-7613(02)00335-7
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745