Open AccessHydrogen sulfide exposure induces NLRP3 inflammasome‐dependent IL‐1β and IL‐18 secretion in human mononuclear leukocytes in vitro
Author(s) -
Basic Amina,
Alizadehgharib Sara,
Dahlén Gunnar,
Dahlgren Ulf
Publication year - 2017
Publication title -
clinical and experimental dental research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.464
H-Index - 9
ISSN - 2057-4347
DOI - 10.1002/cre2.69
Subject(s) - inflammasome , sodium hydrosulfide , peripheral blood mononuclear cell , secretion , monocyte , chemistry , interleukin , cell culture , cytokine , microbiology and biotechnology , in vitro , hydrogen sulfide , biochemistry , immunology , biology , sulfur , receptor , genetics , organic chemistry
The aim was to investigate if hydrogen sulfide (H 2 S) induces the formation of the NLRP3 inflammasome and subsequent IL‐1β and IL‐18 secretion in human peripheral blood mononuclear cells (PBMCs) and in the human monocyte cell line THP1. Bacterial production of H 2 S has been suggested to participate in the inflammatory host response in periodontitis pathogenesis. H 2 S is a toxic gas with pro‐inflammatory properties. It is produced by bacterial degradation of sulfur‐containing amino acids, for example, cysteine. We hypothesize that H 2 S affects the inflammatory host response by inducing formation of the NLRP3 inflammasome and thereby causes the secretion of IL‐1ß and IL‐18. PBMCs from eight healthy blood donors, the human monocyte cell line THP1 Null, and two variants of the THP1 cell line unable to form the NLRP3 inflammasome were cultured in the presence or absence of 1 mM sodium hydrosulfide (NaHS) in 24‐well plates at 37°C for 24 hr. Supernatants were collected and the IL‐1β and IL‐18 concentrations were measured with DuoSet ELISA Development kit. PBMCs exposed to NaHS produced more IL‐1ß and IL‐18 than unexposed control cells ( p = .023 and p = .008, respectively). An increase of extracellular potassium ions (K + ) inhibited the secretion of IL‐1ß and IL‐18 ( p = .008). Further, NaHS triggered the secretion of IL‐1ß and IL‐18 in human THP1‐Null monocytes ( p = .0006 and p = .002, respectively), while the NaHS‐dependent secretion was reduced in the monocyte cell lines unable to form the NLRP3 inflammasome. Hence, the results suggest that NaHS induces the formation of the NLRP3 inflammasome and thus the secretion of IL‐1ß and IL‐18. Enhanced NLRP3 inflammasome‐dependent secretion of IL‐1β and IL‐18 in human mononuclear leukocytes exposed to NaHS in vitro is reported. This may be a mode for H 2 S to contribute to the inflammatory host response and pathogenesis of periodontal disease.