Cell sheets using human amniotic fluid stem cells reduce tissue fibrosis in murine full-thickness skin wounds.
Amniotic Fluid
/ cytology
Animals
Cell Differentiation
Cell Membrane
/ metabolism
Cells, Cultured
Collagen
/ metabolism
Epidermis
/ pathology
Female
Fibrosis
Granulation Tissue
/ pathology
Humans
Immunophenotyping
Male
Mice, Inbred BALB C
Skin
/ pathology
Stem Cells
/ cytology
Tissue Engineering
Wound Healing
Amniotic fluid stem cell
Cell sheet
Fibrosis
Scar formation
Wound healing
Journal
Tissue & cell
ISSN: 1532-3072
Titre abrégé: Tissue Cell
Pays: Scotland
ID NLM: 0214745
Informations de publication
Date de publication:
Feb 2021
Feb 2021
Historique:
received:
16
08
2020
revised:
24
11
2020
accepted:
25
11
2020
pubmed:
29
12
2020
medline:
11
8
2021
entrez:
28
12
2020
Statut:
ppublish
Résumé
The use of mesenchymal stem cell sheets is a promising strategy for skin regeneration. The injection of dissociated human amniotic fluid stem cells (hAFSCs) was recently found to accelerate cutaneous wound healing with reduced fibrotic scarring, similar to fetal wound healing. However, the use of hAFSCs in applications of cell sheet technology remains limited. The aim of this study was to determine the in vivo efficacy of in vitro-cultured hAFSC sheets in wound healing. The cell sheets were characterized by immunohistochemistry and RT-qPCR and grafted onto full-thickness wounds in BALB/c mice. The wound size was measured, and re-epithelialization, granulation tissue area, and collagen content of the regenerated wound were analyzed histologically. Although the hAFSC sheet contained abundant extracellular matrix molecules and expressed high levels of anti-fibrotic mediators, its grafting did not affect wound closure or the size of the granulation tissue area. In contrast, the organization of type I collagen bundles in the regenerated wound was markedly reduced, while the levels of type III collagen were increased after implantation of the hAFSC sheet. These results suggest that hAFSC sheets can exert anti-fibrotic properties without delaying wound closure.
Identifiants
pubmed: 33360545
pii: S0040-8166(20)30630-3
doi: 10.1016/j.tice.2020.101472
pii:
doi:
Substances chimiques
Collagen
9007-34-5
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
101472Informations de copyright
Copyright © 2020 Elsevier Ltd. All rights reserved.