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Article
Nature Immunology  4, 321 - 329 (2003)
Published online: 3 March 2003; | doi:10.1038/ni907

Plasma cell differentiation and the unfolded protein response intersect at the transcription factor XBP-1

Neal N. Iwakoshi1, 4, Ann-Hwee Lee1, 4, Prasanth Vallabhajosyula1, Kevin L. Otipoby2, Klaus Rajewsky2 & Laurie H. Glimcher1, 3

1  Department of Immunology and Infectious Diseases, Harvard School of Public Health 651 Huntington Avenue, Boston, Massachusetts 02115-6017, USA.

2  Center for Blood Research, Harvard Medical School, Boston, Massachusetts 02115, USA.

3  Department of Medicine, Harvard Medical School, Boston, Massachusetts 02115, USA.

4  These authors contributed equally to this work.

Correspondence should be addressed to Laurie H. Glimcher lglimche@hsph.harvard.edu
The transcription factor X-box binding protein 1 (XBP-1) is essential for the differentiation of plasma cells and the unfolded protein response (UPR). Here we show that UPR-induced splicing of XBP-1 by the transmembrane endonuclease IRE1 is required to restore production of immunoglobulin in XBP-1-/- mouse B cells, providing an integral link between XBP-1, the UPR and plasma cell differentiation. Signals involved in plasma cell differentiation, specifically interleukin-4, control the transcription of XBP-1, whereas its post-transcriptional processing is dependent on synthesis of immunoglobulins during B cell differentiation. We also show that XBP-1 is involved in controlling the production of interleukin-6, a cytokine that is essential for plasma cell survival. Thus, signals upstream and downstream of XBP-1 integrate plasma cell differentiation with the UPR.

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Nature Immunology
ISSN: 1529-2908
EISSN: 1529-2916
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