Journal article

High rate of antibody secretion is not integral to plasma cell differentiation as revealed by XBP-1 deficiency

N Taubenheim, DM Tarlinton, S Crawford, LM Corcoran, PD Hodgkin, SL Nutt

Journal of Immunology | Published : 2012

Abstract

During B cell terminal differentiation, a complex set of transcription factors interact to drive the phenotypic and functional changes leading to the development of Ab-secreting cells (ASCs). The transcription factor X-box binding protein 1 (XBP-1) is an essential part of one of the branches of the unfolded protein response (UPR). The UPR is induced when a cell has to handle large amounts of proteins, as is the case in ASCs. Although XBP-1 was initially also ascribed an indispensable function in plasma cell development, later studies of B cell-specific deletion reported a much milder consequence of XBP-1 deficiency. Our interest was to determine whether XBP-1 was integral for the differentia..

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Grants

Awarded by National Health and Medical Research Council of Australia


Funding Acknowledgements

This work was supported by grants (575500) and fellowships from the National Health and Medical Research Council of Australia (to D. M. T., P. D. H., S.L.N.) and an Australian Research Council Future Fellowship (to S.L.N.). This work was made possible through Victorian State Government Operational Infrastructure Support and the Australian government National Health and Medical Research Council Independent Research Institute Infrastructure Support Scheme.