Cutting edge: suppressor of cytokine signaling 3 inhibits activation of NFATp

A Banerjee, AS Banks, MC Nawijn… - The Journal of …, 2002 - journals.aai.org
A Banerjee, AS Banks, MC Nawijn, XP Chen, PB Rothman
The Journal of Immunology, 2002journals.aai.org
Recent studies have suggested that signaling initiated by the activation of Ag receptors and
signaling activated through cytokine receptors may be regulated by a common set of
inhibitory proteins. Suppressor of cytokine signaling 3 (SOCS-3), which has previously been
demonstrated to inhibit cytokine signaling, is induced on TCR ligation. Overexpression of
SOCS-3 can inhibit transcription driven by the IL-2 promoter in response to T cell activation.
This inhibitory activity correlates with the suppression of calcineurin-dependent …
Abstract
Recent studies have suggested that signaling initiated by the activation of Ag receptors and signaling activated through cytokine receptors may be regulated by a common set of inhibitory proteins. Suppressor of cytokine signaling 3 (SOCS-3), which has previously been demonstrated to inhibit cytokine signaling, is induced on TCR ligation. Overexpression of SOCS-3 can inhibit transcription driven by the IL-2 promoter in response to T cell activation. This inhibitory activity correlates with the suppression of calcineurin-dependent dephosphorylation and activation of the IL-2 promoter binding transcription factor, NFATp. Infection of primary murine T cells with a retrovirus encoding SOCS-3 blocks their IL-2 production in response to activation. Interestingly, SOCS-3 was found to coimmunoprecipitate with the catalytic subunit of calcineurin. These studies suggest that SOCS-3 may regulate T cell function as part of a negative feedback loop.
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