The Production Mechanism of TNF-alpha and IL-6 by Group IIA Phospholipase A2.
	    		
		   		
		   			
		   		
	    	
    	 
    	10.12701/yujm.2004.21.2.177
   		
        
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Jae Hong AHN
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Dae Won PARK
			        		
			        		;
		        		
		        		
		        		
			        		Jin Hee KIM
			        		
			        		;
		        		
		        		
		        		
			        		Jei Jun BAE
			        		
			        		;
		        		
		        		
		        		
			        		Yeun Kyoung BAE
			        		
			        		;
		        		
		        		
		        		
			        		Yoon Ki PARK
			        		
			        		
		        		
		        		
		        		
		        		
		        			
			        		
			        		Author Information
			        		
		        		
		        		
			        		
			        		
			        			1. Department of Obstetrics and Gynecology, College of Medicine, Yeungnam University, Daegu, Korea. yoonki@med.yu.ac.kr
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Original Article
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		Group IIA phospholipase A2;
			        		
			        		
			        		
				        		TNF-alpha;
			        		
			        		
			        		
				        		IL-6;
			        		
			        		
			        		
				        		Macrophage cells;
			        		
			        		
			        		
				        		Inflammation
			        		
			        		
	        			
        			
        		
 
        	
            
            	- MeSH:
            	
	        			
	        				
	        				
				        		
					        		Animals;
				        		
			        		
				        		
					        		Enzyme-Linked Immunosorbent Assay;
				        		
			        		
				        		
					        		Fatty Acids;
				        		
			        		
				        		
					        		Group II Phospholipases A2*;
				        		
			        		
				        		
					        		HEK293 Cells;
				        		
			        		
				        		
					        		Inflammation;
				        		
			        		
				        		
					        		Interleukin-6*;
				        		
			        		
				        		
					        		Macrophages;
				        		
			        		
				        		
					        		Mice;
				        		
			        		
				        		
					        		Phospholipases A2, Secretory;
				        		
			        		
				        		
					        		Phospholipids;
				        		
			        		
				        		
					        		Plasma;
				        		
			        		
				        		
					        		Plasmids;
				        		
			        		
				        		
					        		RNA, Messenger;
				        		
			        		
				        		
					        		Tumor Necrosis Factor-alpha*
				        		
			        		
	        			
	        			
            	
            	
 
            
            
            	- From:Yeungnam University Journal of Medicine
	            		
	            		 2004;21(2):177-190
	            	
            	
 
            
            
            	- CountryRepublic of Korea
 
            
            
            	- Language:Korean
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	BACKGROUND: Secretory phospholipase A2 (sPLA2) are a group of extracellular enzymes that release fatty acids at the sn-2 position of phospholipids. Group IIA sPLA2 (sPLA2-IIA) has been detected in the inflammatory fluids, and its plasma level increases in the inflammatory disease. This study examined the effect of sPLA2-IIA on mouse macropahges in order to investigate the potential mechanism of sPLA2-induced inflammation. MATERIALS AND METHODS: Wild type PLA2 and mutant H48Q PLA2 were purified from HEK293 cells transfected with the corresponding plasmids, and the PLA2 activities were measured using 1-palmitoyl-2-[1- (14) C]linoleoyl-3-phosphatidylethanolamine as substrates. The TNF-alpha and IL-6 released in the supernatants were determined by ELISA. In addition, the TNF-alpha and IL-6 mRNA were analyzed by RT-PCR. RESULTS: sPLA2-IIA stimulated the production of TNF-alpha and IL-6 in a dose- and time-dependent manner. In addition, the effect of sPLA2-IIA on cytokine production from the macrophage was found to be associated with the accumulation of their specific mRNA. The mRNA levels of TNF-alpha and IL-6 peaked at 2 and 6 hours in a time-dependent manner, respectively. CONCLUSION: In conclusion, the production of proinflammatory cytokine might be mediated by the binding of sPLA2-IIA to the receptors.