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Asian Sand Dust Increases MUC8 and MUC5B Expression via TLR4-Dependent ERK2 and P38 MAPK in Human Airway Epithelial Cells
Dept. of Otorhinolaryngology-Head and Neck Surgery, Yeungnam Univ. College of Medicine
Hyung-Gyun NA, Hyung-Gyun NA, Chang-hwi PARK, Yo Han CHOI, Hoon-Sung KIM, Joon Kon KIM, Yoon Seok CHOI, Chang Hoon BAE, Si-Youn SONG, Yong-Dae KIM
¸ñÀû: To investigate the effect and signaling pathway of ASD on mucin expressions in human airway epithelial cells. ¹æ¹ý:In the NCI-H292 cells and the primary cultures of human nasal epithelial cells, the effect and signaling pathway of ASD on MUC8 and MUC5B expressions were investigated using reverse transcriptase-polymerase chain reaction (RT-PCR), real-time PCR, enzyme immunoassay, and immunoblot analysis with several specific inhibitors and small interfering RNA (siRNA). °á°ú:ASD increased MUC8 and MUC5B expressions, and activated the phosphorylations of extracellular signal-regulated kinase 1/2 (ERK1/2) and p38 mitogen-activated protein kinase (MAPK). U0126 (ERK1/2 MAPK inhibitor) and SB203580 (p38 MAPK inhibitor) inhibited ASD-induced MUC8 and MUC5B expressions. In addition, knockdowns of ERK2 and p38 MAPK by siRNA blocked ASD-induced MUC8 and MUC5B mRNA expressions. Toll-like receptor 4 (TLR4) mRNA expression was increased after treatment with ASD. Knockdown of TLR4 by siRNA blocked ASD-induced MUC8 and MUC5B mRNA expressions. Furthermore, the phosphorylations of ERK1/2 and p38 MAPK were blocked by knockdown of TLR4. °á·Ð:These results show that ASD induces MUC8 and MUC5B expressions via TLR4-dependent ERK2 and p38 MAPK signaling pathway in human airway epithelial cells.


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