Figure 1.
Figure 1. NFAT activation following TCR stimulation. TCR stimulation leads to calcium flux and additional signaling events that result in the activation of calcineurin, a Ca+2-calmodulin–dependent phosphatase that dephosphorylates NFAT proteins, enabling their movement to the nucleus (NFATc1-c4). Once in the nucleus, NFATc1 to NFATc4 cooperate with various coactivators (NFATn) to promote gene transcription. NFAT kinases, such as GSK-3, rephosphorylate NFATc1 to c4, thus leading to their relocalization to the cytoplasm.

NFAT activation following TCR stimulation. TCR stimulation leads to calcium flux and additional signaling events that result in the activation of calcineurin, a Ca+2-calmodulin–dependent phosphatase that dephosphorylates NFAT proteins, enabling their movement to the nucleus (NFATc1-c4). Once in the nucleus, NFATc1 to NFATc4 cooperate with various coactivators (NFATn) to promote gene transcription. NFAT kinases, such as GSK-3, rephosphorylate NFATc1 to c4, thus leading to their relocalization to the cytoplasm.

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