The classical
pathway for activation of NF-kB, a key transcriptional regulator of the immune
system, is controlled by the IKK complex. Activated IKK phosphorylates IkB
which is ubiquitinated and rapidly degraded, allowing NF-kB to translocate from
the cytoplasm to the nucleus where it activates gene
transcription. However, the mechanisms regarding IKK activation have been
elusive.
Now CARMA1, Bcl-10,
and MALT1 are helping to fill in the blanks of IKK activation. These
proteins are downstream of the T cell receptor (TCR) and upstream of the IKK
complex (Fig. 1). Antigen-TCR signaling in the adaptive immune system leads to
PKC-q activation and formation of an oligomerization-ubiquitination
(Ub)-phosphorylation (P) pathway leading to activated IKK. Oligomerization-Ub-P
pathways have also been found to mediate NF-kB activation through TLR
(Toll-like receptor) signaling; suggesting these emerging IKK activation
pathways may play key roles in regulating both adaptive and innate immunity.
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