- Author:
	        		
		        		
		        		
			        		Mi Hee PARK
			        		
			        		
			        		
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			        		Yu Jin JUNG
			        		
			        		;
		        		
		        		
		        		
			        		Pyeung Hyeun KIM
			        		
			        		
		        		
		        		
		        		
			        		
			        		Author Information
			        		
 - Publication Type:Original Article
 - Keywords: TLR; LPS; M6-395; CpG-ODN; AID; Ig class switch recombination
 - MeSH: B-Lymphocytes; Cell Proliferation; Germ Cells; Immunoglobulin A; Immunoglobulin Class Switching; Immunoglobulin G; Oligodeoxyribonucleotides; Recombination, Genetic; Toll-Like Receptors
 - From:Immune Network 2012;12(1):27-32
 - CountryRepublic of Korea
 - Language:English
 - Abstract: BACKGROUND: Toll-like receptors (TLRs) have been extensively studied in recent years. However, functions of these molecules in murine B cell biology are largely unknown. A TLR4 stimulant, LPS is well known as a powerful polyclonal activator for murine B cells. METHODS: In this study, we explored the effect of a murine TLR9 stimulant, M6-395 (a synthetic CpG ODNs) on B cell proliferation and Ig production. RESULTS: First, M6-395 was much more potent than LPS in augmenting B cell proliferation. As for Ig expression, M6-395 facilitated the expression of both TGF-beta1-induced germ line transcript alpha (GLTalpha) and IL-4-induced GLTgamma1 as levels as those by LPS and Pam3CSK4 (TLR1/2 agonist) : a certain Ig GLT expression is regarded as an indicative of the corresponding isotype switching recombination. However, IgA and IgG1 secretion patterns were quite different--these Ig isotype secretions by M6-395 were much less than those by LPS and Pam3CSK4. Moreover, the increase of IgA and IgG1 production by LPS and Pam3CSK4 was virtually abrogated by M6-395. The same was true for the secretion of IgG3. We found that this unexpected phenomena provoked by M6-395 is attributed, at least in part, to its excessive mitogenic nature. CONCLUSION: Taken together, these results suggest that M6-395 can act as a murine polyclonal activator but its strong mitogenic activity is unfavorable to Ig isotype switching.
 
            
