Literature DB >> 15933053

The development of functional B lymphocytes in conditional PU.1 knock-out mice.

Matthew Polli1, Aleksandar Dakic, Amanda Light, Li Wu, David M Tarlinton, Stephen L Nutt.   

Abstract

An abundance of research has entrenched the view that the Ets domain containing transcription factor PU.1 is fundamental to the development and function of B lymphocytes. In this study, we have made use of a conditional PU.1 allele to test this notion. Complete deletion of PU.1 resulted in the loss of B cells and all other lineage-positive cells in the fetal liver and death between E18.5 and birth; however, specific deletion of PU.1 in the B lineage had no effect on B-cell development. Furthermore, deletion of PU.1 in B cells did not compromise their ability to establish and maintain an immune response. An increased level of apoptosis was observed in vitro upon B-cell receptor (BCR) cross-linking; however, this was partially rescued by interleukin-4 (IL-4). These findings suggest that PU.1 is not essential for the development of functional B lymphocytes beyond the pre-B stage.

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Year:  2005        PMID: 15933053     DOI: 10.1182/blood-2005-01-0283

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  31 in total

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9.  Sox4 is required for the survival of pro-B cells.

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Journal:  J Immunol       Date:  2013-01-23       Impact factor: 5.422

10.  IRF8 regulates B-cell lineage specification, commitment, and differentiation.

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