Suppressive Effects of 4-(Phenylsulfanyl) Butan-2-One on CCL-1 Production via Histone Acetylation in Monocytes.
Ming-Kai TsaiMei-Lan TsaiZhi-Hong WenWei-Ting LiaoYi-Ching LinHsin-Ying Clair ChiouMing-Hong LinChih-Hsing HungPublished in: Current issues in molecular biology (2022)
The 4-(phenylsulfanyl) butan-2-one (4-PSB-2), a marine-derived compound from soft coral, was proven to have multiple biological activities including neuroprotection and potent anti-inflammatory effects. CC chemokine ligand (CCL)-1 belongs to T helper (Th)2-related chemokines that are involved in the recruitment of Th2 inflammatory cells. Histone acetylation has been recognized as a critical mechanism underlying the regulated cytokine and chemokine production. Our study tried to investigate the anti-inflammatory effect of 4-PSB-2 on CCL-1 production in human monocytes and explore possible underlying intracellular processes, including epigenetic regulation. To confirm our hypothesis, human monocyte THP-1 cell line and primary CD14 + cells were pretreated with various concentrations of 4-PSB-2 and then were stimulated with lipopolysaccharide (LPS). The CCL-1 concentration was measured by enzyme-linked immunosorbent assays, and the intracellular signaling pathways and epigenetic regulation of 4-PSB-2 were investigated by using Western blotting and chromatin immunoprecipitation analysis. In this study, we found that 4-PSB-2 had a suppressive effect on LPS-induced CCL-1 production. Moreover, this suppressive effect of 4-PSB-2 was mediated via intracellular signaling such as the mitogen-activated protein kinase and nuclear factor-κB pathways. In addition, 4-PSB-2 could suppress CCL-1 production by epigenetic regulation through downregulating histone H3 and H4 acetylation. In short, our study demonstrated that 4-PSB-2 may have a potential role in the treatment of allergic inflammation.
Keyphrases
- lps induced
- liver injury
- liver fibrosis
- induced apoptosis
- endothelial cells
- inflammatory response
- anti inflammatory
- nuclear factor
- dendritic cells
- oxidative stress
- drug induced
- dna methylation
- signaling pathway
- transcription factor
- gene expression
- reactive oxygen species
- cell cycle arrest
- peripheral blood
- cell death
- cell proliferation
- endoplasmic reticulum stress
- combination therapy
- high speed