Tuesday, 6 December 2011: 13:30 - 13:45
Tulum (Cancún Center)
Ruan Cox Jr.
,
Internal Medicine, University of South Florida, Tampa, FL
Salman Aljubran, MD
,
Allergy and immunology, University of South Florida, Tampa, FL
Richard F. Lockey, MD
,
Division of Allergy & Immunology, University of South Florida and James A. Haley Veterans' Hospital, Tampa, FL
Narasaiah Kolliputi, PhD
,
Internal Medicine, University of South Florida, Tampa, FL
Background: The inflammasome is a multi-protein complex which regulates the activation of caspase-1. This activation results in the cleavage and secretion of the IL-1
β super family cytokines, IL-1
β, IL-18, and IL-33. NLR family-pyrin domain containing- 3 (NLRP3) is a nucleotide binding domain-leucine rich repeat (NLR) family protein responsible for sensitization and oligomerization of the NLRP3 inflammasome complex. Although various damage and pathogen associated patterns have been implicated as stimuli, the exact mechanism of activation has yet to be elucidated. Capase-5, an inflammatory caspase with similar homology to caspase-1, is a key molecule activation of the NLRP1 inflammasome. Caspase-4, an evolutionary duplicate in humans to murine caspase 12 along with caspase 5, is important in IL-1
β processing; its involvement with the NLRP3 inflammasome is unknown. We therefore investigated whether caspase-4 plays a role in the activation of the NLRP3 inflammasome.
Methods: Inflammasomes in THP-1 macrophages were activated using Nigericin (10ug/mL), a bacterial pore causing toxin and NLRP3 inflammasome activator, in the presence or absence of various concentrations (0.1µM,1µM, and 10µM) of caspase-4 inhibitor, Z-YVAD-FMK. We analyzed the inflammasome activation, caspase-1 cleavage, and IL-1β release by western blot and ELISA analysis.
Results: Our results indicate that inhibition of caspase-4 leads to a dose dependant decrease in IL-1β secretion. In addition, our results show that caspase-4 contributes to IL-1β and caspase-1 cleavage, both of which are hall marks of inflammasome activation.
Conclusions: These findings suggest that caspase-4 is important to the activation of the NLRP3 inflammasome. In modulating the inflammasome, caspase-4 appears to be a druggable target for treatment of chronic inflammatory pulmonary conditions such as allergy and asthma.
