EXOGENOUS TRANSFORMING GROWTH-FACTOR-BETA AMPLIFIES ITS OWN EXPRESSION AND INDUCES SCAR FORMATION IN A MODEL OF HUMAN FETAL SKIN REPAIR
EXOGENOUS TRANSFORMING GROWTH-FACTOR-BETA AMPLIFIES ITS OWN EXPRESSION AND INDUCES SCAR FORMATION IN A MODEL OF HUMAN FETAL SKIN REPAIR
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DOI:
10.1097/00000658-199508000-00006
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发表时间:
1995-08-01
影响因子:
9
通讯作者:
ADZICK, NS
中科院分区:
文献类型:
--
作者:
LIN, RY;SULLIVAN, KM;ADZICK, NS
ObjectiveFetal skin wounds heal without scarring. To determine the role of IGF-beta(1) in fetal wound healing, mRNA expression of TGF-beta(1) was analyzed in human fetal and adult skin wounds.MethodsHuman fetal skin transplanted to a subcutaneous location on an adult athymic mouse that was subsequently wounded heals without scar, whereas human adult skin heals with scar formation in that location. In situ hybridization for TGF-beta(1) mRNA expression and species-specific immunohistochemistry for fibroblasts, macrophages, and neutrophils were performed in human adult wounds, fetal wounds, and fetal wounds treated with a TGF-beta(1) slow release disk.ResultsTransforming growth factor-beta(1) mRNA expression was induced by wounding adult skin. No TGF-beta(1) mRNA upregulation was detected in human fetal skin after wounding. However, when exogenous TGF-beta(1) was added to human fetal skin, induction of TGF-beta(1) mRNA expression in human fetal fibroblasts occurred, an adult-like inflammatory response was detected, and the skin healed with scar formation.ConclusionsTransforming growth factor-beta(1) is an important modulator in scar formation. Anti-TGF-beta(1) strategies may promote scarless healing in adult wounds.