Extended Culture of Bone Marrow with Granulocyte Macrophage-Colony Stimulating Factor Generates Immunosuppressive Cells.
	    		
		   		
		   			
		   		
	    	
    	- Author:
	        		
		        		
		        		
			        		Hye Young NA
			        		
			        		
			        		
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			        		Moah SOHN
			        		
			        		;
		        		
		        		
		        		
			        		Seul Hye RYU
			        		
			        		;
		        		
		        		
		        		
			        		Wanho CHOI
			        		
			        		;
		        		
		        		
		        		
			        		Hyunju IN
			        		
			        		;
		        		
		        		
		        		
			        		Hyun Soo SHIN
			        		
			        		;
		        		
		        		
		        		
			        		Chae Gyu PARK
			        		
			        		
		        		
		        		
		        		
			        		
			        		Author Information
			        		
 - Publication Type:Brief Communication
 - Keywords: Bone marrow; Dendritic cells; Granulocyte-macrophage colony-stimulating factor; Lymphocyte culture test, mixed; Immunosuppression
 - MeSH: Bone Marrow*; Dendritic Cells; Granulocyte-Macrophage Colony-Stimulating Factor; Granulocytes*; Immunosuppression; Lymphocyte Culture Test, Mixed; Major Histocompatibility Complex; T-Lymphocytes
 - From:Immune Network 2018;18(2):e16-
 - CountryRepublic of Korea
 - Language:English
 - Abstract: Bone marrow-derived dendritic cells (BM-DCs) are generated from bone marrow (BM) cells cultured with granulocyte macrophage-colony stimulating factor (GM-CSF) for a week. In this study we investigated the effect of duration on the BM culture with GM-CSF. Within several months, the cells in the BM culture gradually expressed homogeneous levels of CD11c and major histocompatibility complex II on surface, and they became unable to stimulate allogeneic naïve T cells in mixed lymphocyte reaction (MLR). In addition, when the BM culture were sustained for 32 wk or longer, the BM cells acquired ability to suppress the proliferation of allogeneic T cells in MLR as well as the response of ovalbumin-specific OT-I transgenic T cells in antigen-dependent manner. We found that, except for programmed death-ligand 1, most cell surface molecules were expressed lower in the BM cells cultured with GM-CSF for the extended duration. These results indicate that BM cells in the extended culture with GM-CSF undergo 2 distinct steps of functional change; first, they lose the immunostimulatory capacity; and next, they gain the immunosuppressive ability.
 
            