| Literature DB >> 11460154 |
A M Reimold1, N N Iwakoshi, J Manis, P Vallabhajosyula, E Szomolanyi-Tsuda, E M Gravallese, D Friend, M J Grusby, F Alt, L H Glimcher.
Abstract
Considerable progress has been made in identifying the transcription factors involved in the early specification of the B-lymphocyte lineage. However, little is known about factors that control the transition of mature activated B cells to antibody-secreting plasma cells. Here we report that the transcription factor XBP-1 is required for the generation of plasma cells. XBP-1 transcripts were rapidly upregulated in vitro by stimuli that induce plasma-cell differentiation, and were found at high levels in plasma cells from rheumatoid synovium. When introduced into B-lineage cells, XBP-1 initiated plasma-cell differentiation. Mouse lymphoid chimaeras deficient in XBP-1 possessed normal numbers of activated B lymphocytes that proliferated, secreted cytokines and formed normal germinal centres. However, they secreted very little immunoglobulin of any isotype and failed to control infection with the B-cell-dependent polyoma virus, because plasma cells were markedly absent. XBP-1 is the only transcription factor known to be selectively and specifically required for the terminal differentiation of B lymphocytes to plasma cells.Entities:
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Year: 2001 PMID: 11460154 DOI: 10.1038/35085509
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962