Comparison of skeletal muscle decellularization protocols and recellularization with adipose-derived stem cells for tissue engineering

Decellularization is a novel technique employed for scaffold manufacturing, as a strategy for skeletal muscle (SM) tissue engineering applications. However, poor decellularization efficacy is still a problem for the use of decellularized scaffolds as truly biocompatible biomaterials. For recellulari...

Full description

Saved in:
Bibliographic Details
Published inBiologicals Vol. 86; p. 101767
Main Authors Esposito, Joyce, Cunha, Pricila da Silva, Martins, Thaís Maria da Mata, Melo, Mariane Izabella Abreu de, Sá, Marcos Augusto de, Gomes, Dawidson Assis, Góes, Alfredo Miranda de
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.05.2024
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Decellularization is a novel technique employed for scaffold manufacturing, as a strategy for skeletal muscle (SM) tissue engineering applications. However, poor decellularization efficacy is still a problem for the use of decellularized scaffolds as truly biocompatible biomaterials. For recellularization, adipose-derived stem cells (ASCs) are a good option, due to their immunomodulatory and pro-regenerative capacity, but few studies have described their combination with muscle-decellularized matrices (mDMs). This work aimed to evaluate the efficiency of four multi-step decellularization protocols to produce mDMs and to investigate in vitro biocompatibility with ASCs. Here, we described the different efficacies of muscle decellularization methods, suggesting the need for stricter standardization of the method, considering the large range of applications in SM tissue engineering, which is also a promising platform for preclinical studies with rat disease models using autologous cells.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1045-1056
1095-8320
1095-8320
DOI:10.1016/j.biologicals.2024.101767