Effects of heat stimulation and L-ascorbic acid 2-phosphate supplementation on myogenic differentiation of artificial skeletal muscle tissue constructs

被引:19
作者
Ikeda, Kazushi [1 ]
Ito, Akira [2 ]
Sato, Masanori [2 ]
Kanno, Shota [2 ]
Kawabe, Yoshinori [2 ]
Kamihira, Masamichi [1 ,2 ]
机构
[1] Kyushu Univ, Grad Sch Syst Life Sci, Fukuoka, Japan
[2] Kyushu Univ, Dept Chem Engn, Fukuoka, Japan
基金
日本学术振兴会;
关键词
skeletal muscle tissue engineering; C2C12; cells; heat stimulation; magnesium ascorbyl phosphate; myogenic differentiation; contractile force; VITAMIN-C; ENGINEERING TECHNIQUE; PROTEIN PHOSPHATASE; SHOCK PROTEINS; MOUSE MUSCLE; STEM-CELL; IN-VITRO; CALCINEURIN; EXPRESSION; HYPERTROPHY;
D O I
10.1002/term.2030
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Although skeletal muscle tissue engineering has been extensively studied, the physical forces produced by tissue-engineered skeletal muscles remain to be improved for potential clinical utility. In this study, we examined the effects of mild heat stimulation and supplementation of a L-ascorbic acid derivative, L-ascorbic acid 2-phosphate (AscP), on myoblast differentiation and physical force generation of tissue-engineered skeletal muscles. Compared with control cultures at 37 degrees C, mouse C2C12 myoblast cells cultured at 39 degrees C enhanced myotube diameter (skeletal muscle hypertrophy), whereas mild heat stimulation did not promote myotube formation (differentiation rate). Conversely, AscP supplementation resulted in an increased differentiation rate but did not induce skeletal muscle hypertrophy. Following combined treatment with mild heat stimulation and AscP supplementation, both skeletal muscle hypertrophy and differentiation rate were enhanced. Moreover, the active tension produced by the tissue-engineered skeletal muscles was improved following combined treatment. These findings indicate that tissue culture using mild heat stimulation and AscP supplementation is a promising approach to enhance the function of tissue-engineered skeletal muscles. Copyright (C) 2015 John Wiley & Sons, Ltd.
引用
收藏
页码:1322 / 1331
页数:10
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