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Nat Immunol. 2005 Mar;6(3):303-13. Epub 2005 Feb 13.

STAT5 regulates the self-renewal capacity and differentiation of human memory B cells and controls Bcl-6 expression.

Author information

1
Department of Cell Biology and Histology of the Academic Medical Center, University of Amsterdam, 1105 AZ Amsterdam, Netherlands.

Abstract

It is unknown how B cells that mature during a germinal center reaction 'decide' between plasma or memory cell fate. Here we describe a previously unknown subpopulation of B cells in the human germinal center that is characterized by tyrosine phosphorylated transcriptional activator STAT5. These cells had an activated centrocyte phenotype and had abundant expression of BCL6 but low expression of PRDM1, both encoding transcriptional repression proteins. Using RNA interference and ectopic expression of constitutively activated forms of STAT5, we demonstrate here a function for STAT5 in the self-renewal of B cells in vitro. STAT5b isoform seemed to directly upregulate Bcl-6, and ectopic expression of Bcl-6 in B cells resulted in self-renewal and inhibition of plasma cell differentiation. These data indicate that activation of STAT5 is involved in regulation of memory B cell differentiation.

PMID:
15711548
DOI:
10.1038/ni1172
[Indexed for MEDLINE]

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