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Benzyl Isothiocyanate Attenuates Inflammasome Activation in <i>Pseudomonas aeruginosa</i> LPS-Stimulated THP-1 Cells and Exerts Regulation through the MAPKs/NF-κB Pathway
oleh: Won Sun Park, Jeonghan Lee, Giyoun Na, SaeGwang Park, Su-Kil Seo, Jung Sik Choi, Won-Kyo Jung, Il-Whan Choi
Format: | Article |
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Diterbitkan: | MDPI AG 2022-01-01 |
Deskripsi
Inflammasomes are a group of intracellular multiprotein platforms that play important roles in immune systems. Benzyl isothiocyanate (BITC) is a constituent of cruciferous plants and has been confirmed to exhibit various biological activities. The modulatory effects of BITC on inflammasome-mediated interleukin (IL)-1β expression and its regulatory mechanisms in <i>Pseudomonas aeruginosa</i> (<i>P. aeruginosa</i>) LPS/ATP-stimulated THP-1 cells was investigated. Monocytic THP-1 cells were treated with phorbol myristate acetate (PMA) to induce differentiation into macrophages. Enzyme-linked immunosorbent assays (ELISA) were performed to measure the levels of IL-1β produced in <i>P. aeruginosa</i> LPS/ATP-exposed THP-1 cells. Western blotting was performed to examine the BITC modulatory mechanisms in inflammasome-mediated signaling pathways. BITC inhibited IL-1β production in <i>P. aeruginosa</i> LPS/ATP-induced THP-1 cells. BITC also inhibited activation of leucine-rich repeat protein-3 (NLRP3) and caspase-1 in <i>P. aeruginosa</i> LPS/ATP-induced THP-1 cells. Furthermore, we show that mitogen-activated protein kinase (MAPK) and nuclear factor-κB (NF-κB) activation in <i>P. aeruginosa</i> LPS was attenuated by BITC. These BITC-mediated modulatory effects on IL-1β production may have therapeutic potential for inflammasome-mediated disorders such as a nasal polyp.