Photopolymerizable Hydrogel-Encapsulated Fibromodulin-Reprogrammed Cells for Muscle Regeneration

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Departmental Papers (Dental)
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Fibromodulin
Fibromodulin-reprogrammed cells
Myogenesis
Photopolymerizable hydrogel
Cell Differentiation
Cells
Cultured
Fibromodulin
Humans
Hydrogels
Muscle Development
Muscle
Skeletal
Regeneration
Satellite Cells
Skeletal Muscle
chitosan derivative
collagen type 1
fibromodulin
hydrogel
methacrylated glycol chitosan
MyoD1 protein
myogenic factor 5
myogenin
myosin
myosin heavy chain
myosin heavy chain 1
myosin heavy chain 2
transcription factor PAX7
unclassified drug
apoptosis
BJ [Human fibroblast] cell line
bone development
cell differentiation
cell encapsulation
cell reprogramming technique
cell spreading
cell survival
cell viability
cellular distribution
chondrogenesis
controlled study
evidence based practice
gene expression profiling
graft recipient
histogenesis
human
human cell
immunofluorescence
in vitro study
male
microenvironment
muscle development
muscle regeneration
muscle tissue
myotube
Note
priority journal
skeletal muscle
skeletal muscle cell
skeletal muscle satellite cell
tenogenesis
tissue engineering
cell culture
hydrogel
muscle development
regeneration
skeletal muscle
skeletal muscle satellite cell
Dentistry
Endodontics and Endodontology
Oral Biology and Oral Pathology
Other Dentistry
Periodontics and Periodontology
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Yang, Pu
Li, Chenshuang
Lee, Min
Marzvanyan, Anna
Zhao, Zhihe
Ting, Kang
Soo, Chia
Zheng, Zhong
Contributor
Abstract

A central challenge in tissue engineering is obtaining a suitable cell type with a capable delivery vehicle to replace or repair damaged or diseased tissues with tissue mimics. Notably, for skeletal muscle tissue engineering, given the inadequate availability and regenerative capability of endogenous myogenic progenitor cells as well as the tumorigenic risks presented by the currently available pluri- and multipotent stem cells, seeking a safe regenerative cell source is urgently demanded. To conquer this problem, we previously established a novel reprogramming technology that can generate multipotent cells from dermal fibroblasts using a single protein, fibromodulin (FMOD). The yield FMOD-reprogrammed (FReP) cells exhibit exceeding myogenic capability without tumorigenic risk, making them a promising and safe cell source for skeletal muscle establishment. In addition to using the optimal cell for implantation, it is equally essential to maintain cellular localization and retention in the recipient tissue environment for critical-sized muscle tissue establishment. In this study, we demonstrate that the photopolymerizable methacrylated glycol chitosan (MeGC)/type I collagen (ColI)hydrogel provides a desirable microenvironment for encapsulated FReP cell survival, spreading, extension, and formation of myotubes in the hydrogel three-dimensionally in vitro, without undesired osteogenic, chondrogenic, or tenogenic differentiation. Furthermore, gene profiling revealed a paired box 7 (PAX7) / myogenic factor 5 (MYF5) / myogenic determination 1 (MYOD1) / myogenin (MYOG) / myosin cassette elevation in the encapsulated FReP cells during myogenic differentiation, which is similar to that of the predominant driver of endogenous skeletal muscle regeneration, satellite cells. These findings constitute the evidence that the FReP cell-MeGC/ColI-hydrogel construct is a promising tissue engineering mimic for skeletal muscle generation in vitro, and thus possesses the extraordinary potential for further in vivo validation. © 2020 Mary Ann Liebert Inc.. All rights reserved.

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2020-10-01
Journal title
Tissue Engineering - Part A.
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