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IKK? negatively regulates ASC-dependent inflammasome activation.


ABSTRACT: The inflammasomes are multiprotein complexes that activate caspase-1 in response to infections and stress, resulting in the secretion of pro-inflammatory cytokines. Here we report that I?B kinase ? (IKK?) is a critical negative regulator of apoptosis-associated specklike protein containing a C-terminal caspase-activation-andrecruitment (CARD) domain (ASC)-dependent inflammasomes. IKK? controls the inflammasome at the level of the adaptor ASC, which interacts with IKK? in the nucleus of resting macrophages in an IKK? kinase-dependent manner. Loss of IKK? kinase activity results in inflammasome hyperactivation. Mechanistically, the downstream nuclear effector IKK-related kinase (IKKi) facilitates translocation of ASC from the nucleus to the perinuclear area during inflammasome activation. ASC remains under the control of IKK? in the perinuclear area following translocation of the ASC/IKK? complex. Signal 2 of NLRP3 activation leads to inhibition of IKK? kinase activity through the recruitment of PP2A, allowing ASC to participate in NLRP3 inflammasome assembly. Taken together, these findings reveal a IKKi-IKK?-ASC axis that serves as a common regulatory mechanism for ASC-dependent inflammasomes.

SUBMITTER: Martin BN 

PROVIDER: S-EPMC4298287 | biostudies-literature | 2014 Sep

REPOSITORIES: biostudies-literature

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The inflammasomes are multiprotein complexes that activate caspase-1 in response to infections and stress, resulting in the secretion of pro-inflammatory cytokines. Here we report that IκB kinase α (IKKα) is a critical negative regulator of apoptosis-associated specklike protein containing a C-terminal caspase-activation-andrecruitment (CARD) domain (ASC)-dependent inflammasomes. IKKα controls the inflammasome at the level of the adaptor ASC, which interacts with IKKα in the nucleus of resting m  ...[more]

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