Effect of zinc ion on the expression of osteoblastic proteins in MC3T3-E1 cells in inflammatory environment
	    		
		   		
		   			
		   		
	    	
    	 
    	10.3760/cma.j.issn.1002-0098.2016.08.010
   		
        
        	
        		- VernacularTitle:锌离子对炎症微环境下成骨细胞成骨相关蛋白表达的影响
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Jizhou TAN
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Ermin NIE
			        		
			        		;
		        		
		        		
		        		
			        		Chunyuan ZHANG
			        		
			        		;
		        		
		        		
		        		
			        		Rui JIANG
			        		
			        		
		        		
		        		
		        		
		        		
		        			
			        		
			        		Author Information
			        		
		        		
		        		
			        		
			        		
			        			1. 中山大学附属第一医院口腔科
			        		
		        		
	        		
        		 
        	
        	
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		Zinc sulfate;
			        		
			        		
			        		
				        		Inflammasomes;
			        		
			        		
			        		
				        		Osteoblasts;
			        		
			        		
			        		
				        		Peri-implantitis
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Chinese Journal of Stomatology
	            		
	            		 2016;51(8):486-490
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
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		        	Abstract:
			       	
			       		
				        
				        	Objective To investigate the effect of zinc ion on the expression of osteoblastic proteins.Methods Mice osteoblasts MC3T3-E1 cells were subcultured.Inflammatory environment model was established by tumor necrosis factor α(TNF-αt) at a concentration of 10 mg/L.According to different concentration of Zn2+,the cells were divided into TNF-α group,control group,group A(TNF-α+ 10-4 mol/L Zn2+),group B(TNF-α+ 10-5 mol/L Zn2+),group C(TNF-α+10-6 mol/L Zn2+).After 24,48,and 72 h of culture,cell counting kit-8(CCK-8) assay was used to analyze the proliferation of the cells.ALP activity was examined.Bone morphogenetic protein-2(BMP-2),Runt-related transcription factor 2(RUNX2),Osterix and receptor activator of NF-κB ligand(RANKL) protein levels were determined by Western blotting after 72 h of culture.Results The cells grew by adherence after 24 h.After 72 h,the cells grew dense,and the cells showed long spindle shape or irregular shape.The proliferation of osteoblasts in TNF-α group,group B and group C became lower than that in the control group(P<0.05),and was not significantly different between group A and the control group(P > 0.05).ALP activity examination demonstrated that the groups cultured for 72 h revealed the highest ALP activity and the most prominent differentation compared with 24 h and 48 h groups.ALP activity was significantly decreased in TNF-α group,group B and group C compared with control group(P<0.05),but was not significantly different between group A and control group(P>0.05).The protein levels of BMP-2,RUNX2 and Osterix were significantly decreased in TNF-α group,group B and group C compared with control group(P<0.05),while showed no significant difference between group A and the control group.Protein level of RANKL was significantly increased in TNF-α group,grope B and group C compared with control group(P<0.05),while showed no significant difference between group A and control group.Conclusions The concentration of 10-4 mol/L Zn2+ can significantly increase the expression of osteoblastic proteins such as ALP,BMP-2,RUNX2,Osterix and decrease the expression of RANKL in mice osteoblasts in TNF-α inflammatory environment.