Effect of 17?-estradiol (E_2) on the gene expression of osteoprotegerin in human osteoblast and MG-63 cells
	    		
		   		
	    	
    	
    	
   		
        
        	
        		- VernacularTitle:雌二醇对成骨细胞护骨素基因表达的影响
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Eryuan LIAO
			        		
			        		;
		        		
		        		
		        		
			        		Houde ZHOU
			        		
			        		;
		        		
		        		
		        		
			        		Xiaoge DENG
			        		
			        		
		        		
		        		
		        		
		        		
		        		
			        		
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Journal Article
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		Osteoblast;
			        		
			        		
			        		
				        		Estradiol;
			        		
			        		
			        		
				        		Osteoprotegerin
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Chinese Journal of Endocrinology and Metabolism
	            		
	            		 1986;0(04):-
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	Objective  To investigate the effects of 17  ?  estradiol (E  2) on the gene expression of osteoprotegerin (OPG) in human osteoblast (HOB) and MG  63 osteosarcoma cell lines at various maturity stages of cultures, and to make a better understanding of the mechanism of E  2 deficient osteoporosis. Methods  The activities of alkaline phosphatase (ALP), osteocalcin (OC) secreted by cultured cells at different stages of cell proliferation, maturity and collagen mineralization, as well as the effect of E  2 on the OPG gene expression were determined. HOB was prepared from ilial bone tissue in adults, OPG gene expression was quantified by RT  PCR, and the activity of ALP, OC was corrected with Bradford′s method. Results  For both kinds of cells, expression of OPG at the 12th days′ culture reached the highest levels without any treatment, and 10    -8   mol/LofE  2increasedOPGmRNA to a maximum of about 10 times (P