Construction of directional differentiation model from mouse embryonic stem cells to Leydig-like cells in vitro.
- Author:
	        		
		        		
		        		
			        		Ying-ying ZHANG
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Ya-dong HUANG
			        		
			        		;
		        		
		        		
		        		
			        		Ren-shan GE
			        		
			        		;
		        		
		        		
		        		
			        		Dan-yan ZHU
			        		
			        		
		        		
		        		
		        		
			        		
			        		Author Information
			        		
 - Publication Type:Journal Article
 - MeSH: Animals; Cell Differentiation; drug effects; genetics; Cell Line; Embryonic Stem Cells; cytology; metabolism; Leydig Cells; cytology; metabolism; Male; Mice; Steroidogenic Factor 1; genetics; Transfection
 - From: Journal of Zhejiang University. Medical sciences 2012;41(4):386-392
 - CountryChina
 - Language:Chinese
 - 
		        	Abstract:
			       	
			       		
				        
				        	
OBJECTIVETo construct a directional differentiation model from mouse embryonic stem cells into leydig-like cells in vitro.
METHODSMouse ES-D3 cells were transfected with plasmid containing steroidogenic factor 1 (SF-1) gene, then treated with RA and 8Br-cAMP, while the cells transfected with empty plasmid were used as the negative controls. The morphology of leydig-like cells differentiated from ES-D3 cells was observed with light microscopy. The expression levels of StAR, P450scc and 3β-HSD were detected by RT-PCR, Western Blot and fluorescence microscopy analysis in leydig-like cells derived from the ES cells.
RESULTSES-D3 cells were transfected with plasmid containing SF-1 gene successfully, and SF-1 was expressed 24 h after transfection. The SF-1-transfected ES-D3 cells were induced by RA and 8Br-cAMP to differentiate into leydig-like cells. The differentiated cells showed spindle shape with tentacles, which expressed the specific protein marker for leydig cells 3β-HSD1 and P450scc. Meanwhile, in these leydig-like cells, the expression of StAR increased compared with control group. 3β-HSD1, P450scc and StAR were not detected in negative control group.
CONCLUSIONWhen the ES-D3 cells are transfected with SF-1 plasmid and then treated with RA and 8Br-cAMP, the cells are able to differentiate into leydig-like cells, indicating that the model of directional differentiation of ES cells into leydig-like cells has been constructed successfully.
 
            