Study on the collagen constitution of hyperplastic scar in different ages and its influencing factors.
- Author:
Lin QIU
1
;
Xian-qing JIN
;
Dai-li XIANG
;
Yue-xian FU
;
Xiao-fei TIAN
Author Information
- Publication Type:Journal Article
- MeSH: Adolescent; Adult; Age Factors; Burns; metabolism; pathology; Child; Child, Preschool; Cicatrix, Hypertrophic; metabolism; pathology; Collagen Type I; biosynthesis; Collagen Type III; biosynthesis; Female; Humans; Infant; Male; Matrix Metalloproteinase 1; biosynthesis; Middle Aged; Tissue Inhibitor of Metalloproteinase-1; biosynthesis; Transforming Growth Factor beta1; biosynthesis; Young Adult
- From: Chinese Journal of Burns 2003;19(4):236-240
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the collagen constitution of hyperplastic scar (HS) in different ages and the change of relative factors.
METHODSThirty cases with HS were divided into two groups according to patients' age: group 1 (1 - 19 years, A) and group 2 (20 - 50 years, B). The normal skin (NS) from corresponding age of volunteers was employed as control group. The changes in TGFbeta1, collagenase (MMP-1) and tissue inhibitor of metalloproteinase (TIMP-1beta) and the collagen ratio were observed by means of in situ hybridization technique and SABC (Strept-Avidin-Biotin complex) immunohistochemistry and image analysis.
RESULTSThe ratio of type I to type III collagen in A group was 6.48 in average and 3.76 in B group, but there was no evident difference in the ratio during the disease process in both groups. The expression of TGFbeta1 in A group was much higher than that in B group (P < 0.01). The TIMP-1 mRNA expression showed no difference among all age groups in HS patients, but it was much higher than that in NS group. The MMP-1 expression was evidently lower than TIMP-1 expression, and there was no difference in MMP-1 expression compared with NS group.
CONCLUSION(1) The TGFbeta1 expression in HS patients was negatively correlated with age, and the increased expression of TGFbeta1 produced an increase ratio of type I to type III collagen. (2) High level expression of TIMP-1 led to the formation of HS by inhibiting MMP-1 expression, and the expression was not related to age.
