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. 1993 Apr 1;177(4):1215-9.
doi: 10.1084/jem.177.4.1215.

T cell-dependent induction of NF-kappa B in B cells

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T cell-dependent induction of NF-kappa B in B cells

A C Lalmanach-Girard et al. J Exp Med. .

Abstract

In comparison to B cell stimulation mediated by surface immunoglobulin (Ig) antigen receptor ligation, little is known about the intracellular events associated with T cell-dependent B cell responses. A model for the efferent phase of T cell-B cell interaction was used to examine the capacity of activated T cells to trigger nuclear expression of the trans-acting transcription factor, NF-kappa B, in B cells. Fixed, activated, but not fixed, resting Th2 cells were found to induce increased binding activity for a kappa B site-containing oligonucleotide in a time-dependent manner. This induction of NF-kappa B was eliminated by an antibody directed against a 39-kD cell interaction protein on activated T cells as well as by a soluble form of B cell CD40. Of particular relevance to intracellular signaling, NF-kappa B induction was not diminished by prior depletion of B cell protein kinase C (PKC) with phorbol myristate acetate. These results strongly suggest that T cell-dependent B cell stimulation is associated with NF-kappa B induction via p39-CD40 interaction and that this is brought about by non-PKC dependent signaling, in marked contrast to the previously documented requirement for PKC in sIg receptor-mediated stimulation. This suggest that NF-kappa B responds to more than one receptor-mediated intracellular signaling pathway in B cells and may be part of a "final common pathway" for B cell stimulation.

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References

    1. Anal Biochem. 1976 May 7;72:248-54 - PubMed
    1. J Immunol. 1991 May 1;146(9):2921-7 - PubMed
    1. J Cell Physiol. 1986 Dec;129(3):347-55 - PubMed
    1. Annu Rev Immunol. 1987;5:175-99 - PubMed
    1. Proc Natl Acad Sci U S A. 1987 Dec;84(23):8588-92 - PubMed

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