Polyopes affinis Suppressed IFN-γ- and TNF-α-Induced Inflammation in Human Keratinocytes via Down-Regulation of the NF-κB and STAT1 Pathways.
Yuna HaWon-Hwi LeeJang Kyun KimHee-Kyung JeonChang Seok LeeYoun-Jung KimPublished in: Molecules (Basel, Switzerland) (2022)
Polyopes affinis is a red algal species commonly found on the South coast and near Jeju Island, Korea. This study aimed to determine whether P. affinis extracts can inhibit the pathogenesis of T-helper-2 (Th2)-mediated inflammation in a human keratinocyte cell line of atopic dermatitis (AD). Cells were incubated with 10 ng/mL of interferon gamma (IFN-γ) and 10 ng/mL of tumor necrosis factor-alpha (TNF-α) at various concentrations of PAB (10, 30, and 60 µg/mL) and PAA (100, 500, and 1000 µg/mL) extracts. A gene-ontology (GO)-enrichment analysis revealed that PAB significantly enriched the genes associated with biological processes such as cell adhesion, immune response, inflammation, and chemokine-mediated pathways. PAB suppressed the expression of the secretory proteins and mRNAs that are associated with the thymus and the production of activation-regulated chemokines (TARC/CCL17) and macrophage-derived chemokines (MDC/CCL22). The effect of the extract on mitogen-activated protein kinases (MAPKs) was related to its inhibition of TARC/CCL17 and MDC/CCL22 production by blocking NF-κB and STAT1 activation. These results suggest that seaweed extract may improve AD by regulating pro-inflammatory chemokines. In conclusion, we first confirmed the existence of phloroglucinol, a polyphenol formed from a precursor called phlorotannin, which is present in PAB, and this result proved the possibility of PAB being used as a treatment for AD.
Keyphrases
- oxidative stress
- immune response
- dendritic cells
- induced apoptosis
- liver injury
- diabetic rats
- endothelial cells
- liver fibrosis
- drug induced
- rheumatoid arthritis
- cell adhesion
- signaling pathway
- atopic dermatitis
- high glucose
- cell proliferation
- induced pluripotent stem cells
- lps induced
- poor prognosis
- pluripotent stem cells
- adipose tissue
- nuclear factor
- single cell
- regulatory t cells
- toll like receptor
- gene expression
- copy number
- binding protein
- replacement therapy
- genetic diversity
- genome wide identification