Mol. Cell. Biol., Sep 1996, 4591-4603, Vol 16, No. 9
SC Lin and J Stavnezer
Interaction between CD40 on B cells and CD40 ligand (CD40L) on T cells has
been shown to mediate T-cell contact help for B-cell proliferation,
differentiation, and immunoglobulin isotype switching. It has recently been
shown that cross-linking CD40 on mouse B cells induces germ line gamma1 and
epsilon transcripts and that interleukin-4 synergizes with CD40 signaling
to further induce these germ line transcripts. Germ line transcripts have
been shown to be required for class switch recombination. Here we show that
signaling via CD40 increases expression of a transiently transfected
luciferase reporter plasmid driven by the germ line Cgamma1 promoter in
M12.4.1 B-lymphoma cells. By linker-scanning mutation analysis of the
promoter, we have identified a CD40-responsive region (CD40RR) which is
able to confer inducibility by CD40L to a minimal c-fos promoter. The
CD40RR contains three binding sites for NF-kappaB/Rel proteins which are
each required for maximal induction of CD40RR activity by CD40L. Binding of
the NF- kappaB/Rel proteins p50, p65, c-Rel, and RelB to the CD40RR is
induced by CD40 signaling in M12.4.1 cells and in splenic B cells.
Cotransfection of expression plasmids for p50 and p65 or p50 and RelB, but
not c-Rel, into M12.4.1 cells transactivates the CD40RR and the germ line
gamma1 promoter. These data demonstrate that NF-kappaB Rel proteins
activated by CD40 ligation play an important role in induction of the germ
line Cgamma1 promoter.
Copyright © 1996, American Society for Microbiology
Activation of NF-kappaB/Rel by CD40 engagement induces the mouse germ line immunoglobulin Cgamma1 promoter
Department of Molecular Genetics and Microbiology, University of Massachusetts Medical School, Worecester 01655-0122, USA.
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