Obtusifolin isolated from the seeds of Cassia obtusifolia regulates the gene expression and production of MUC5AC mucin in airway epithelial cells via affecting NF-κB pathway.
Byung-Soo ChoiYu-Jin KimJae-Sue ChoiHyun Jae LeeChoong Jae LeePublished in: Phytotherapy research : PTR (2019)
We investigated whether obtusin, obtusifolin, and cassiaside isolated from the seeds of Cassia obtusifolia inhibit the gene expression and production of airway mucin 5AC (MUC5AC). Confluent NCI-H292 cells were pretreated with obtusin, obtusifolin, or cassiaside for 30 min and then stimulated with epidermal growth factor (EGF), phorbol 12-myristate 13-acetate (PMA), or tumor necrosis factor-α (TNF-α) for 24 hr. The MUC5AC mucin gene expression was measured by reverse transcription-polymerase chain reaction. Production of MUC5AC mucin protein was measured by enzyme-linked immunosorbent assay. To elucidate the action mechanism of obtusifolin, effect of obtusifolin on PMA-induced nuclear factor kappa B (NF-κB) signaling pathway was investigated by western blot analysis. Obtusin, obtusifolin, or cassiaside inhibited the expression of MUC5AC mucin gene and the production of MUC5AC mucin protein, induced by EGF, PMA, or TNF-α. Obtusifolin inhibited PMA-induced activation (phosphorylation) of inhibitory kappa B kinase, and thus phosphorylation and degradation of inhibitory kappa B alpha. Obtusifolin inhibited PMA-induced nuclear translocation of NF-κB p65. These results suggest that obtusifolin can regulate the production and gene expression of mucin by acting on airway epithelial cells through regulation of NF-κB signaling pathway.
Keyphrases
- nuclear factor
- gene expression
- signaling pathway
- growth factor
- toll like receptor
- pi k akt
- induced apoptosis
- dna methylation
- high glucose
- rheumatoid arthritis
- diabetic rats
- epithelial mesenchymal transition
- drug induced
- cell cycle arrest
- lps induced
- protein kinase
- oxidative stress
- binding protein
- inflammatory response
- poor prognosis
- high throughput
- transcription factor
- atomic force microscopy
- copy number
- immune response
- genome wide
- cell death
- south africa
- mass spectrometry
- cell proliferation
- amino acid