ERK signaling pathway mediated epithelial-mesenchymal transition induced by SiO₂ in human bronchial epithelial cells.
	    		
		   		
		   			
		   		
	    	
    	 
    	10.3969/j.issn.1672-7347.2011.11.009
   		
        
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Zhenqin GAO
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Yongbin HU
			        		
			        		;
		        		
		        		
		        		
			        		Jingwu PENG
			        		
			        		;
		        		
		        		
		        		
			        		Zhenghao DENG
			        		
			        		;
		        		
		        		
		        		
			        		Guannan LIANG
			        		
			        		;
		        		
		        		
		        		
			        		Haiying JIANG
			        		
			        		;
		        		
		        		
		        		
			        		Jianhua ZHOU
			        		
			        		
		        		
		        		
		        		
		        		
		        			
			        		
			        		Author Information
			        		
		        		
		        		
			        		
			        		
			        			1. Department of Pathology, Xiangya School of Medicine, Central South University, Changsha 410013, China.
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Journal Article
 
        	
        	
            
            	- MeSH:
            	
	        			
	        				
	        				
				        		
					        		Actins;
				        		
			        		
				        		
					        		metabolism;
				        		
			        		
				        		
					        		Bronchi;
				        		
			        		
				        		
					        		cytology;
				        		
			        		
				        		
					        		Cadherins;
				        		
			        		
				        		
					        		metabolism;
				        		
			        		
				        		
					        		Cell Transdifferentiation;
				        		
			        		
				        		
					        		drug effects;
				        		
			        		
				        		
					        		Cells, Cultured;
				        		
			        		
				        		
					        		Epithelial Cells;
				        		
			        		
				        		
					        		cytology;
				        		
			        		
				        		
					        		physiology;
				        		
			        		
				        		
					        		Epithelial-Mesenchymal Transition;
				        		
			        		
				        		
					        		Humans;
				        		
			        		
				        		
					        		MAP Kinase Signaling System;
				        		
			        		
				        		
					        		physiology;
				        		
			        		
				        		
					        		Mitogen-Activated Protein Kinases;
				        		
			        		
				        		
					        		metabolism;
				        		
			        		
				        		
					        		Silicon Dioxide;
				        		
			        		
				        		
					        		pharmacology
				        		
			        		
	        			
	        			
            	
            	
 
            
            
            	- From:
	            		
	            			Journal of Central South University(Medical Sciences)
	            		
	            		 2011;36(11):1085-1089
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	OBJECTIVE:To determine the role of extracellular signal regulated kinase (ERK) signaling pathway in SiO₂ induced epithelial-mesenchymal transition (EMT) in human bronchial epithelial cells (HBEC) in vitro.
				        	
				        
				        	METHODS:HBEC were treated with SiO₂ (0-300 μg/mL) for 72 h or pretreated with U0126 (0-30 μmol/L) for 1 h and then treated with 200 μg/mL SiO₂ for 72 h. Western blot was used to detect the protein expression of E-cadherin and α-smooth muscle actin (α-SMA). The activity of ERK was examined by mitogen-activated protein kinase (MAPK) activity assay kit in HBEC exposing to SiO₂ (200 μg/mL) for 0-8 h.
				        	
				        
				        	RESULTS:The expression of E-cadherin decreased gradually in SiO₂ -stimulated HBEC, and the effect was most significant at 300 μg/mL (P<0.01). The expression of α-SMA increased and the effect was most evident at 200 μg/mL (P<0.01). With SiO₂ treatment, the activity of ERK was upregulated significantly. The phosphorylation of ERK increased at 30 min and decreased after 1 h. U0126 significantly inhibited SiO₂ -induced expression changes in E-cadherin and α-SMA. At 30 μmol/L, the effect was most evident(P<0.01).
				        	
				        
				        	CONCLUSION:ERK signaling pathway mediated EMT induced by SiO₂ in HBEC.