Expressions of programmed death 1 and programmed death ligand 1 in rat model of acute liver failure
	    		
		   		
		   			
		   		
	    	
    	 
    	10.3760/cma.j.issn.1000-6680.2010.09.005
   		
        
        	
        		- VernacularTitle:急性肝功能衰竭大鼠模型中程序性死亡-1及其配体的表达
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Wei HOU
			        		
			        		;
		        		
		        		
		        		
			        		Fengling WANG
			        		
			        		;
		        		
		        		
		        		
			        		Qian JIN
			        		
			        		;
		        		
		        		
		        		
			        		Ying YU
			        		
			        		;
		        		
		        		
		        		
			        		Dan YE
			        		
			        		;
		        		
		        		
		        		
			        		Hongdong XIE
			        		
			        		;
		        		
		        		
		        		
			        		Wenhui TU
			        		
			        		;
		        		
		        		
		        		
			        		Yongping CHEN
			        		
			        		
		        		
		        		
		        		
		        		
		        		
			        		
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Journal Article
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		Liver failure,acute;
			        		
			        		
			        		
				        		Disease models,animal;
			        		
			        		
			        		
				        		RNA,messenger;
			        		
			        		
			        		
				        		Gene expression;
			        		
			        		
			        		
				        		Reverse transcription polymerase chain reaction;
			        		
			        		
			        		
				        		Apoptosis
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Chinese Journal of Infectious Diseases
	            		
	            		 2010;28(9):532-535
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	Objective To study the expressions of programmed death 1 (PD-1) and programmed death ligand 1 (PD-L1) in liver injury of acute liver failure (ALF) in rats and the role of PD-1/ PD-L1 in liver inflammatory injury. Methods SD rats were divided into two groups: 6 in normal group and 30 in ALF model group. The ALF models in rats were induced by D-galactosamine (D-Gal). The sera and hepatic tissue samples were collected at 12, 24, 48, 72 and 120 hours after D-Gal injection. Expressions of PD-1 mRNA and PD-L1 mRNA in hepatic tissue samples were detected by reverse transcription-polymerase chain reaction (RT-PCR). Comparison of measurement data between groups was done by t test. Correlation test was performed using Pearson linear correlation analysis. Results The levels of alanine animotransferase (ALT) and aspartate animotransferase (AST) at 12 h of D-Gal injection were (217. 3±33. 7) U/L and (397. 2± 101.3) U/L, respectively,which were both significantly higher than those in normal group [(30. 5 ±3. 1) U/L and (78. 6±4.2) U/L, respectively; t=-8. 921 and -6. 121, respectively; both P<0.01] and peaked at 48 h.The expression of PD-1 mRNA in model group at 12 h (0. 385±0. 074) was significantly higher than that in normal group (0. 097±0.009) (t= -7. 725, P<0.01) , and peaked at 48 h (0. 927±0. 132),then decreased obviously at 72 h. The expression of PD-L1 mRNA in the liver tissue of normal rats was very little, while that in model group was increased gradually over time, then peaked at 48 h (0. 593±0. 105; t =- 10. 076, P<0. 01). The expressions of PD-1 and PD-L1 were positively correlated with ALT level (r=0. 807 and 0. 792, respectively; both P<0. 01). Conclusion The expressions of PD-1/PD-L1 may play an important role in liver inflammatory injury in rat model of acute liver failure.