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. 1992 Oct 1;176(4):1015-24.
doi: 10.1084/jem.176.4.1015.

Functional characterization of the human tumor necrosis factor receptor p75 in a transfected rat/mouse T cell hybridoma

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Functional characterization of the human tumor necrosis factor receptor p75 in a transfected rat/mouse T cell hybridoma

P Vandenabeele et al. J Exp Med. .

Abstract

We investigated the biological role of the human tumor necrosis factor p75 (hTNF-R75), making use of the species specificity of TNF responses in murine (m) T cell lines. Several TNF-mediated activities on mouse T cells, such as cytokine induction or proliferation, showed a 100-500-fold difference in specific biological activity between mTNF and hTNF. After transfection of hTNF-R75 cDNA in a rat/mouse T cell hybridoma (PC60), however, the 100-fold lower specific biological activity of hTNF was converted to the same specific biological activity as mTNF. The TNF-mediated induction of granulocyte/macrophage colony-stimulating factor was strongly synergized by the addition of interleukin 1. In the presence of the latter cytokine, ligand-competing monoclonal antibodies against hTNF-R75 (utr-1, utr-2, utr-3) were agonistic on transfected PC60 cells. This agonistic activity was further enhanced by crosslinking with sheep anti-murine immunoglobulin antibodies. These data provide direct evidence for a functional role of TNF-R75, without ligand-dependent TNF-R55 involvement, in the induction of cytokine secretion in T cells.

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References

    1. J Exp Med. 1990 Nov 1;172(5):1517-20 - PubMed
    1. Science. 1990 May 25;248(4958):1019-23 - PubMed
    1. J Immunol Methods. 1990 Dec 31;135(1-2):25-32 - PubMed
    1. Annu Rev Immunol. 1989;7:625-55 - PubMed
    1. J Exp Med. 1989 Dec 1;170(6):1859-67 - PubMed

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