Home LiteratureArticle Details
PMID: 9359694 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Estrogen accelerates cutaneous wound healing associated with an increase in TGF-beta1 levels.

Nature medicine ·Vol. 3 ·No. 11 ·1997-11-00 ·Pages 1209-15

Ashcroft GS, Dodsworth J, van Boxtel E, Tarnuzzer RW, Horan MA, Schultz GS, Ferguson MW

Abstract

The cellular and molecular mechanisms underlying the effects of aging on human cutaneous wound healing are poorly understood, and the possible role of reproductive hormones in this process has never been investigated. We report that aging in healthy females was associated with a reduced rate of cutaneous wound healing, but an improved quality of scarring both microscopically and macroscopically, and with reduced levels of transforming growth factor-beta1 (TGF-beta1) immunostaining and steady-state mRNA in the wound. These age-related changes were reversed by the systemic administration of hormone replacement therapy (HRT). Moreover, ovariectomized young female rodents exhibited a marked delay in repair of acute incisional wounds, which was reversed by the topical application of estrogen. The cellular mechanism underlying these changes appears to involve an estrogen-induced increase in latent TGF-beta1 secretion by dermal fibroblasts. These results suggest that both the rate and quality of wound healing depend on reproductive hormone levels.

MeSH Terms
Administration, Topical Adult Aged Animals Cell Division/drug effects Collagen/analysis Disease Models, Animal Estradiol/administration & dosage,therapeutic use Estrogen Replacement Therapy Female Fibroblasts/drug effects Humans Middle Aged Ovariectomy Progesterone/administration & dosage,therapeutic use RNA, Messenger/analysis Rats Rats, Sprague-Dawley Skin/chemistry,injuries Transforming Growth Factor beta/metabolism Wound Healing/drug effects
Chemicals
RNA, Messenger Transforming Growth Factor beta Progesterone Estradiol Collagen
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Ashcroft G S
Cells, Immunology and Development Division, School of Biological Sciences, University of Manchester, UK.
Dodsworth J
van Boxtel E
Tarnuzzer R W
Horan M A
Schultz G S
Ferguson M W
Article Info
Journal
Nature medicine
Abbr.
Nat Med
ISSN
1078-8956
Published
1997-11-00
Pages
1209-15
Language
English
Region
United States
NLM ID
9502015
Subset
IM
Grants
Wellcome Trust · United Kingdom
Corrections
CommentIn
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