pcDNA3.1-osteogenic growth polypeptide eukaryotic expression vector in bone marrow mesenchymal stem cells
	    		
		   		
		   			
		   		
	    	
    	 
    	10.3969/j.issn.1673-8225.2011.36.011
   		
        
        	
        		- VernacularTitle:pcDNA3.1-成骨生长肽真核表达载体在骨髓基质干细胞中的表达
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Gang AN
			        		
			        		;
		        		
		        		
		        		
			        		Songcen Lü
			        		
			        		;
		        		
		        		
		        		
			        		Yashan GUO
			        		
			        		;
		        		
		        		
		        		
			        		Zhen XUE
			        		
			        		;
		        		
		        		
		        		
			        		Qiukui DENG
			        		
			        		
		        		
		        		
		        		
		        		
		        		
			        		
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Journal Article
 
        	
        	
            
            
            	- From:
	            		
	            			Chinese Journal of Tissue Engineering Research
	            		
	            		 2011;15(36):6696-6700
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	BACKGROUND: Osteogenic growth polypeptide (OGP) had clear effect on promoting osteoblast proliferation, differentiation and mature. OBJECTIVE: To explore the expression of OGP gene, which was transfected into rabbit bone marrow mesenchymal stem cells (BMSCs) and to evaluate the effects of OGP on differentiation of rabbit BMSCs. METHODS: pcDNA3.1-OGP was constructed using gene cloning and recombination techniques. Rabbit BMSCs were transfected with pcDNA3.1-OGP mediated by lipofectamine 2000. The transfection positive cell clones were selected with G418. The expression of OGP gene was detected using reverse transcription-polymerase chain reaction analysis on an mRNA level. Differentiation of pcDNA3.1-OGP transfected BMSCs into osteoblast lineage was observed. RESULTS AND CONCLUSION: The pcDNA3.1-OGP plasmid was constructed successful and OGP expression was detected in rabbit BMSCs. Hydroxyproline content was increased, and alkaline phosphatase activity was also increased. These indicate that pcDNA3.1-OGP transfected BMSCs expressed OGP, and could differentiate into osteoblast lineage.