Substance P up-regulates the TGF-beta 1 mRNA expression of human dermal fibroblasts in vitro.
- Author:
	        		
		        		
		        		
			        		Dahai HU
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Bi CHEN
			        		
			        		;
		        		
		        		
		        		
			        		Xiongxinag ZHU
			        		
			        		;
		        		
		        		
		        		
			        		Ke TAO
			        		
			        		;
		        		
		        		
		        		
			        		Chaowu TANG
			        		
			        		;
		        		
		        		
		        		
			        		Jianbo WANG
			        		
			        		
		        		
		        		
		        		
			        		
			        		Author Information
			        		
 - Publication Type:Journal Article
 - MeSH: Cell Division; Cells, Cultured; Dermis; cytology; Fibroblasts; cytology; drug effects; metabolism; Gene Expression; drug effects; Neurokinin-1 Receptor Antagonists; Quinuclidines; pharmacology; RNA, Messenger; Substance P; metabolism; pharmacology; Transforming Growth Factor beta; genetics; Transforming Growth Factor beta1; Up-Regulation
 - From: Chinese Journal of Plastic Surgery 2002;18(4):234-236
 - CountryChina
 - Language:Chinese
 - 
		        	Abstract:
			       	
			       		
				        
				        	
OBJECTIVETo investigate the role of substance P in the formation of hypertrophic scar.
METHODSDermal fibroblasts derived from human normal skin were cultured with substance P alone or together with selective non-peptide NK-1 tachykinin antagonist, L-703, 606 oxalate salt. The effect of substance P on proliferation of fibroblasts was measured by MTT assay. Furthermore, the TGF-beta 1 mRNA expression in the fibroblasts was determined by in situ hybridization and image analysis.
RESULTSSubstance P enhanced fibroblast proliferation dose-dependently, which showed the maximum rate when the concentration of substance P was 25 ng/ml or higher in the culture media. By 48 hours cultured with 25 ng/ml of substance P, the fibroblasts expressed TGF-beta 1 mRNA more significantly than the fibroblasts without substance P. The effects of substance P on both fibroblast proliferation and TGF-beta 1 mRNA expression could be antagonized by L-703, 606 oxalate salt.
CONCLUSIONThe results suggest that substance P may play an important role in phenotype changes of fibroblasts in skin scarring.
 
            