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Bifurcation of signalling in human innate immune pathways to NF-kB and IRF family activation.
Kusiak, Aleksandra; Brady, Gareth.
Afiliación
  • Kusiak A; Trinity Translational Medicine Institute, St James' Campus, Trinity College Dublin, D08 W9RT Dublin, Ireland. Electronic address: kusiaka@tcd.ie.
  • Brady G; Trinity Translational Medicine Institute, St James' Campus, Trinity College Dublin, D08 W9RT Dublin, Ireland. Electronic address: bradyg1@tcd.ie.
Biochem Pharmacol ; 205: 115246, 2022 11.
Article en En | MEDLINE | ID: mdl-36088989
The human innate immune response can be activated through a wide range of stimuli. This multi-faceted system can be triggered by a range of immunostimulants including pathogen-associated molecular patterns (PAMPs) and damage-associated molecular patterns (DAMPs). These stimuli drive intracellular signalling pathways that branch off downstream to activate several distinct transcription factors. The two most impactful of which in innate immune outcomes are the NF-κB and the IRF family members. Both transcription factor families play defining roles in driving inflammation as well as the antiviral response. Pathways leading to their simultaneous activation share common upstream components but eventually distinct regulators which directly facilitate their activation. This review will discuss the current state of knowledge about what is known about how these pathways bifurcate to activate NF-κB and IRF family members.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: FN-kappa B / Moléculas de Patrón Molecular Asociado a Patógenos Límite: Humans Idioma: En Revista: Biochem Pharmacol Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: FN-kappa B / Moléculas de Patrón Molecular Asociado a Patógenos Límite: Humans Idioma: En Revista: Biochem Pharmacol Año: 2022 Tipo del documento: Article