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Cell-autonomous Fas (CD95)/Fas-ligand interaction mediates activation-induced apoptosis in T-cell hybridomas

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Abstract

A NUMBER of murine T-cell hybridomas undergo apoptosis within a few hours of activation by specific antigens, mitogens, antibodies against the T-cell antigen receptor, or a combination of phorbol ester and calcium ionophore1–3. This phenomenon has been extensively studied as a model for clonal deletion in the immune system, in which potentially autoreactive T cells eliminate themselves by apoptosis after activation, either in the thymus4 or in the periphery5. Here we show that the Fas/CD95 receptor, which can transduce a potent apoptotic signal when ligated6,7, is rapidly expressed following activation of T-cell hybridomas, as is its functional, membrane-bound ligand8. Interference with the ensuing Fas/Fas-ligand interaction inhibits activation-induced apoptosis. Because T-cell receptor ligation can induce apoptosis in a single T hybridoma cell, we suggest that the Fas/Fas-ligand interaction can induce cell death in a cell-autonomous manner.

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Brunner, T., Mogil, R., LaFace, D. et al. Cell-autonomous Fas (CD95)/Fas-ligand interaction mediates activation-induced apoptosis in T-cell hybridomas. Nature 373, 441–444 (1995). https://doi.org/10.1038/373441a0

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  • DOI: https://doi.org/10.1038/373441a0

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