Aligned nanofibers of decellularized muscle ECM support myogenic activity in primary satellite cells in vitro.
Animals
Anisotropy
Cattle
Cell Proliferation
Cells, Cultured
DNA
/ analysis
Extracellular Matrix
/ metabolism
Male
Muscle, Skeletal
/ metabolism
Myoblasts
/ metabolism
Nanofibers
/ chemistry
Polyesters
Rats
Rats, Inbred Lew
Regeneration
Stress, Mechanical
Tensile Strength
Tissue Engineering
/ methods
Tissue Scaffolds
/ chemistry
Journal
Biomedical materials (Bristol, England)
ISSN: 1748-605X
Titre abrégé: Biomed Mater
Pays: England
ID NLM: 101285195
Informations de publication
Date de publication:
02 04 2019
02 04 2019
Historique:
pubmed:
28
2
2019
medline:
23
10
2019
entrez:
28
2
2019
Statut:
epublish
Résumé
Volumetric muscle loss (VML) is a loss of over ∼10% of muscle mass that results in functional impairment. Although skeletal muscle possesses the ability to repair and regenerate itself following minor injuries, VML injuries are irrecoverable. Currently, there are no successful clinical therapies for the treatment of VML. Previous studies have treated VML defects with decellularized extracellular matrix (D-ECM) scaffolds derived from either pig urinary bladder or small intestinal submucosa. These therapies were unsuccessful due to the poor mechanical stability of D-ECM leading to quick degradation in vivo. To circumvent these issues, in this manuscript aligned nanofibers of D-ECM were created using electrospinning that mimicked native muscle architecture and provided topographical cues to primary satellite cells. Additionally, combining D-ECM with polycaprolactone (PCL) improved the tensile mechanical properties of the electrospun scaffold. In vitro testing shows that the electrospun scaffold with aligned nanofibers of PCL and D-ECM supports satellite cell growth, myogenic protein expression, and myokine production.
Identifiants
pubmed: 30812025
doi: 10.1088/1748-605X/ab0b06
doi:
Substances chimiques
Polyesters
0
polycaprolactone
24980-41-4
DNA
9007-49-2
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM