Protomyofibroblast Pathway in Early Thermal Burn Healing

Affiliation auteurs!!!! Error affiliation !!!!
TitreProtomyofibroblast Pathway in Early Thermal Burn Healing
Type de publicationJournal Article
Year of Publication2015
AuteursHermanns-Le T, Pierard GE, Jennes S, Pierard-Franchimont C
JournalSKIN PHARMACOLOGY AND PHYSIOLOGY
Volume28
Pagination250-254
Type of ArticleArticle
ISSN1660-5527
Mots-clésBurn injury, Myofibroblast, Protomyofibroblast, Skin, Wound healing
Résumé

Wound healing following partial thickness thermal burns is commonly hampered by the risk of hypertrophic scarring. Skin myofibroblast (MF) density is commonly increased in postburn healing. The transition between fibroblast-like cells and alpha-smooth muscle actin (SMA)+ MF possibly begins with CD14+ monocytes, evolving to CD14+ CD34+ fibrocytes, followed by beta-SMA+ protomyofibroblast (PMF) maturation. Skin biopsies from 25 burn patients were collected about 1 and 4 weeks after injury. Immunohistochemistry was performed using monoclonal antibodies to alpha-SMA, beta-SMA, factor XIIIa, lysozyme, Mac 387, CD14, CD117 and Ulex europaeus agglutinin-1 (UEA-1). The set of Mac 387+ and CD14+ monocytes was accompanied by both CD34+ fibrocytes and factor XIIIa+ dendrocytes. By contrast, beta-SMA+ PMF were rare. Of note, alpha-SMA+ MF were more abundant at week 4 than at week 1 (p < 0.01). The UEA-1+ endothelial cells showed marked variations in their dermal distribution, irrespective of the densities in the other scrutinized cells. In conclusion, healing of partial thickness thermal burns involves a diversity of cell types including PMF. In the present samples, the PMF density remained low. (C) 2015 S. Karger AG, Basel

DOI10.1159/000430102