Human caspase-4 mediates noncanonical inflammasome activation against gram-negative bacterial pathogens
Author(s) -
Cierra N. Casson,
Janet Yu,
Valeria M. Reyes,
Frances Taschuk,
Anjana Yadav,
Alan M. Copenhaver,
Hieu Nguyen,
Ronald G. Collman,
Sunny Shin
Publication year - 2015
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1421699112
Subject(s) - inflammasome , innate immune system , caspase , biology , caspase 1 , complement system , immune system , microbiology and biotechnology , classical complement pathway , aim2 , inflammation , immunology , programmed cell death , apoptosis , genetics
Significance The innate immune system provides a first line of defense against invading pathogens. The inflammasome is an innate immune complex that activates inflammatory caspases upon infection, causing cell death and IL-1 cytokine release, which initiate defense against gram-negative bacterial pathogens but also mediate septic shock. Many inflammasome studies have been performed using cells from mice, but mice and humans differ in their complement of inflammatory caspases. Instead of caspase-11, humans encode the putative orthologs caspase-4 and caspase-5. Here, we show that caspase-4 plays a conserved role in inflammasome activation in response to virulent gram-negative pathogens in primary human macrophages. Our findings provide important insight into how inflammasomes are regulated in human cells.
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