Apoptotic signals delivered through the T-cell receptor of a T-cell hybrid require the immediate–early gene nur77
ZG Liu, SW Smith, KA McLaughlin, LM Schwartz… - Nature, 1994 - nature.com
ZG Liu, SW Smith, KA McLaughlin, LM Schwartz, BA Osborne
Nature, 1994•nature.comENGAGEMENT of the T-cell antigen receptor (TCR) on immature thymic T cells induces
death by apoptosis1–3. Although several lines of evidence indicate that apoptosis requires
de novo gene expression, little is known about the molecular pathways that mediate this
response. Here we show that nur77 (refs 4–7), a zinc-finger transcription factor, is expressed
in response to TCR engagement in immature T cells and T-cell hybrids. Antisense inhibition
of nur77 expression prevents apoptosis in TCR-stimulated cells. nur77 is also expressed in …
death by apoptosis1–3. Although several lines of evidence indicate that apoptosis requires
de novo gene expression, little is known about the molecular pathways that mediate this
response. Here we show that nur77 (refs 4–7), a zinc-finger transcription factor, is expressed
in response to TCR engagement in immature T cells and T-cell hybrids. Antisense inhibition
of nur77 expression prevents apoptosis in TCR-stimulated cells. nur77 is also expressed in …
Abstract
ENGAGEMENT of the T-cell antigen receptor (TCR) on immature thymic T cells induces death by apoptosis1–3. Although several lines of evidence indicate that apoptosis requires de novo gene expression, little is known about the molecular pathways that mediate this response. Here we show that nur77 (refs 4–7), a zinc-finger transcription factor, is expressed in response to TCR engagement in immature T cells and T-cell hybrids. Antisense inhibition of nur77 expression prevents apoptosis in TCR-stimulated cells. nur77 is also expressed in response to mitogens, but in this case transcription is regulated by 5' upstream elements that are distinct from those used for induction of apoptosis. In addition, polyadenylation is only observed on nur77 transcripts found in condemned cells. These data support a role for nur77 in cell death that may be distinct from that of activation.
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