Signaling pathways downstream of pattern-recognition receptors and their cross talk

MS Lee, YJ Kim - Annu. Rev. Biochem., 2007 - annualreviews.org
MS Lee, YJ Kim
Annu. Rev. Biochem., 2007annualreviews.org
Pattern-recognition receptors (PRRs) initiate innate immunity through pathogen recognition.
Serum PRRs opsonize pathogens for enhanced phagocytic clearance. Toll-like receptors
(TLRs) initiate common NF-κB/AP-1 and distinct IRF3/7 pathways to coordinate innate
immunity and to initiate adaptive immunity against diverse pathogens. Cytoplasmic caspase-
recruiting domain (CARD) helicases, such as RIG-I/MDA5, mediate antiviral immunity by
inducing the production of type I interferons via the adaptor IPS-1, whereas nucleotide …
Abstract
Pattern-recognition receptors (PRRs) initiate innate immunity through pathogen recognition. Serum PRRs opsonize pathogens for enhanced phagocytic clearance. Toll-like receptors (TLRs) initiate common NF-κB/AP-1 and distinct IRF3/7 pathways to coordinate innate immunity and to initiate adaptive immunity against diverse pathogens. Cytoplasmic caspase-recruiting domain (CARD) helicases, such as RIG-I/MDA5, mediate antiviral immunity by inducing the production of type I interferons via the adaptor IPS-1, whereas nucleotide-binding oligomerization domain (NOD)-like receptors mediate mainly antibacterial immunity by activating NF-κB or inflammasomes. Dectin-1 is important for antifungal immunity, promoting phagocytosis and activating NF-κB. Potentially harmful TLR signaling pathways can be negatively regulated by negative feedback mechanisms and also by anti-inflammatory factors such as TGFβ, interleukin (IL)-10, and steroids. Many combinations of TLR-TLR and TLR-NOD modulate inflammatory responses. TLRs and NALP3 interplay to produce mature IL-1β. Thus signaling pathways downstream of PRRs and their cross talk control immune responses in effective manners.
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