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Human decellularized adipose matrix derived hydrogel assists mesenchymal stem cells delivery and accelerates chronic wound healing

Authors :
Youbai Chen
Zhang Bowen
Yan Han
Quan Zeng
Xuetao Pei
Jiafei Xi
Yudi Han
Wen Yue
Jun Shu
Hai-Yang Wang
Ran Tao
Zhaoyang Chen
Source :
Journal of biomedical materials research. Part AREFERENCES. 109(8)
Publication Year :
2020

Abstract

Biological scaffolds based stem cell delivery methods have emerged as a promising approach for tissue repair and regeneration. Here we developed a hydrogel biological scaffold from human decellularized adipose matrix (hDAM) for human adipose-derived stem cells (hASCs) delivery to accelerate chronic wound healing. The hDAM hydrogel was prepared by pepsin mediated digestion and pH controlled neutralization. The morphology, survival, proliferation and angiogenic paracrine activity of hASCs cultured in the hydrogel were assessed. Moreover, the therapeutic efficacy of the hASCs-hydrogel composite for impaired wound healing was evaluated by using a full-thickness wound model on diabetic mouse. The developed hDAM hydrogel was a thermosensitive hydrogel, presented the biochemical complexity of native extracellular matrix (ECM) and formed a porous nanofiber structure after gelation. The hydrogel can support hASCs adhesion, survival and proliferation. Compared to standard culture condition, hASCs cultured in the hydrogel exhibited enhanced paracrine activity with increased secretion of hepatocyte growth factor (HGF). In the diabetic mice model with excisional full-thickness skin wounds, mice treated with the hASCs-hydrogel composite displayed accelerated wound closure and increased neovascularization. Our results suggested that the developed hDAM hydrogel can provide a favorable microenvironment for hASCs with augmented regeneration potential to accelerate chronic wound healing. This article is protected by copyright. All rights reserved.

Details

ISSN :
15524965
Volume :
109
Issue :
8
Database :
OpenAIRE
Journal :
Journal of biomedical materials research. Part AREFERENCES
Accession number :
edsair.doi.dedup.....b1255f50cf2be3adb751febffbd3c6a7