Can leg ulcer fibroblasts phenotype be influenced by human amniotic membrane extract?

Affiliation auteurs!!!! Error affiliation !!!!
TitreCan leg ulcer fibroblasts phenotype be influenced by human amniotic membrane extract?
Type de publicationJournal Article
Year of Publication2014
AuteursTauzin H., Robin S., Humbert P., Viennet C., Saas P., Courderot-Masuyer C., Muret P.
JournalCELL AND TISSUE BANKING
Volume15
Pagination251-255
Date PublishedJUN
Type of ArticleArticle
ISSN1389-9333
Mots-clésExtract, Human amniotic membrane, in vitro, Leg ulcer, Primary fibroblasts
Résumé

Prevalence of leg ulcer in general population is important and new efficient treatments are now needed, especially for chronic leg ulcers. Human amniotic membrane (HAM) can be used as an alternative treatment for recalcitrant leg ulcers. The aim of this study is to investigate the effects of a HAM extract on normal fibroblasts (NF) and ulcer fibroblasts (UF). NF and UF were obtained from biopsies by explants technique. HAM extract was used at 10 mu g of total proteins per ml. Single patient-matched NF and UF were compared, without or with HAM extract. Studied parameters were proliferation rate, retraction of free-floating lattices, alpha smooth muscle actin expression by flow cytometry, and synthesis of elastin, glycosaminoglycans (GAGs), pro-collagen I, MMP-1 and TIMP-1. Our results show that UF had a specific phenotype compared to NF: low proliferation, high expression of alpha-SM actin and high synthesis of MMP-1, TIMP-1 and elastin. HAM extract significantly increased the synthesis of GAGs, pro-collagen I and MMP-1 in NF and decreased retraction of free lattices. HAM extract transiently increased UF proliferation, slowed down lattices retraction and decreased elastin synthesis. In conclusion, HAM extract has little effect on UF for the parameters studied and NF are more responsive than UF. However, clinical beneficial effect of HAM application on leg ulcers was previously observed and might rather be related to an action on keratinocytes and/or a modulation of the highly inflammatory environment of these chronic wounds.

DOI10.1007/s10561-014-9422-4