Expression of the pluripotent molecule TNF in a focused and antigen-restricted fashion might provide an advantage to the host organism. Given the central role of T cells in antigen-specific immunity, we examined whether activated T cells express TNF on their cell surface. FACS analysis of highly purified normal human T cells labeled with an anti-TNF mAb revealed that T cells express cell surface TNF when signaled with the synergistic combination of a calcium ionophore, ionomycin, and a protein kinase C activator, 12-o-tetradecanoyl phorbol acetate. Cell surface radioiodination studies of stimulated T cells demonstrated the presence of 26-kD transmembrane protein, a size predicted by TNF cDNA and different from that of the 17-kD secreted TNF molecule. The induced cell surface expression of TNF could be blocked with cyclosporine and/or methylprednisolone, and Northern analysis for TNF-specific transcripts revealed that this inhibitory effect occurs pretranslationally. Our demonstration for the first time that stimulated normal human T cells display cell surface TNF provides a mechanistic basis for the realization of effects of TNF in an antigen-specific fashion.
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1 March 1990
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March 01 1990
A novel addition to the T cell repertory. Cell surface expression of tumor necrosis factor/cachectin by activated normal human T cells.
M Kinkhabwala,
M Kinkhabwala
Rogosin Institute, Department of Medicine, Cornell University Medical College, New York, New York 10021.
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P Sehajpal,
P Sehajpal
Rogosin Institute, Department of Medicine, Cornell University Medical College, New York, New York 10021.
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E Skolnik,
E Skolnik
Rogosin Institute, Department of Medicine, Cornell University Medical College, New York, New York 10021.
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D Smith,
D Smith
Rogosin Institute, Department of Medicine, Cornell University Medical College, New York, New York 10021.
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V K Sharma,
V K Sharma
Rogosin Institute, Department of Medicine, Cornell University Medical College, New York, New York 10021.
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H Vlassara,
H Vlassara
Rogosin Institute, Department of Medicine, Cornell University Medical College, New York, New York 10021.
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A Cerami,
A Cerami
Rogosin Institute, Department of Medicine, Cornell University Medical College, New York, New York 10021.
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M Suthanthiran
M Suthanthiran
Rogosin Institute, Department of Medicine, Cornell University Medical College, New York, New York 10021.
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M Kinkhabwala
Rogosin Institute, Department of Medicine, Cornell University Medical College, New York, New York 10021.
P Sehajpal
Rogosin Institute, Department of Medicine, Cornell University Medical College, New York, New York 10021.
E Skolnik
Rogosin Institute, Department of Medicine, Cornell University Medical College, New York, New York 10021.
D Smith
Rogosin Institute, Department of Medicine, Cornell University Medical College, New York, New York 10021.
V K Sharma
Rogosin Institute, Department of Medicine, Cornell University Medical College, New York, New York 10021.
H Vlassara
Rogosin Institute, Department of Medicine, Cornell University Medical College, New York, New York 10021.
A Cerami
Rogosin Institute, Department of Medicine, Cornell University Medical College, New York, New York 10021.
M Suthanthiran
Rogosin Institute, Department of Medicine, Cornell University Medical College, New York, New York 10021.
Online ISSN: 1540-9538
Print ISSN: 0022-1007
J Exp Med (1990) 171 (3): 941–946.
Citation
M Kinkhabwala, P Sehajpal, E Skolnik, D Smith, V K Sharma, H Vlassara, A Cerami, M Suthanthiran; A novel addition to the T cell repertory. Cell surface expression of tumor necrosis factor/cachectin by activated normal human T cells.. J Exp Med 1 March 1990; 171 (3): 941–946. doi: https://doi.org/10.1084/jem.171.3.941
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