TY - JOUR
T1 - Plasma cell differentiation requires the transcription factor XBP-1
AU - Reimold, Andreas M.
AU - Iwakoshi, Neal N.
AU - Manis, John
AU - Vallabhajosyula, Prashanth
AU - Szomolanyi-Tsuda, Eva
AU - Gravallese, Ellen M.
AU - Friend, Daniel
AU - Grusby, Michael J.
AU - Alt, Frederick
AU - Glimcher, Laurie H.
PY - 2001/7/19
Y1 - 2001/7/19
N2 - 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.
AB - 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.
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U2 - 10.1038/35085509
DO - 10.1038/35085509
M3 - Article
C2 - 11460154
AN - SCOPUS:0035913294
SN - 0028-0836
VL - 412
SP - 300
EP - 307
JO - Nature
JF - Nature
IS - 6844
ER -