Mechanisms of NLRP1-Mediated Autoinflammatory Disease in Humans and Mice |
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Authors: | Chien-Hsiung Yu Jonas Moecking Matthias Geyer Seth L Masters |
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Institution: | 1. Inflammation Division, The Walter and Eliza Hall Institute of Medical Research, Parkville, VIC 3052, Australia;2. Department of Medical Biology, University of Melbourne, Parkville, VIC 3010, Australia;3. Department of Structural Immunology, Institute of Innate Immunity, University of Bonn, 53127 Bonn, Germany |
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Abstract: | NLRP1 was the first NOD-like receptor described to form an inflammasome, recruiting ASC to activate caspase-1, which processes interleukin-1β and interleukin-18 to their active form. A wealth of new genetic information has now redefined our understanding of this innate immune sensor. Specifically, rare loss-of-function variants in the N-terminal pyrin domain indicate that this part of NLRP1 is autoinhibitory and normally acts to prevent a familial autoinflammatory skin disease associated with cancer. In the absence of a ligand to trigger human NLRP1, these mutations have now confirmed the requirement of NLRP1 autolytic cleavage within the FIIND domain, which had previously been implicated in NLRP1 activation. Autolytic cleavage generates a C-terminal fragment of NLRP1 containing the CARD domain which then forms an ASC-dependent inflammasome. The CARD domain as an inflammasome linker is consistent with the observation that under some conditions, particularly for mouse NLRP1, caspase-1 can be engaged directly, and although it is no longer processed, it is still capable of producing mature IL-1β. Additional rare variants in a linker region between the LRR and FIIND domains of NLRP1 also cause autoinflammatory disease in both humans and mice. This new genetic information is likely to provide for more mechanistic insight in the years to come, contributing to our understanding of how NLRP1 functions as an innate immune sensor of infection and predisposes to autoimmune or autoinflammatory diseases. |
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Keywords: | PRR pattern recognition receptor CARD caspase activation and recruitment domain PYD pyrin domain ASC apoptosis-associated speck-like protein containing a CARD FIIND the “function-to-find” domain NACHT domain present in NAIP CIITA HET-E and TEP1 NLR NOD-like receptor NOD2 nucleotide-binding oligomerization domain-containing protein 2 NR100 N-terminal domain of rodent NLRP1 of approximately 100 amino acids LeTx anthrax lethal toxin LF anthrax lethal factor LRR leucine-rich repeat MDP muramyl dipeptide HEK293T human embryonic kidney cells RIP2 receptor-interacting serine/threonine-protein kinase 2 inflammasome NLRP1 caspase-1 IL-1β autoinflammation |
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