Cardiac Meets Skeletal: What's New in Microfluidic Models for Muscle Tissue Engineering

被引:32
|
作者
Visone, Roberta [1 ]
Gilardi, Mara [2 ,3 ]
Marsano, Anna [4 ,5 ]
Rasponi, Marco [1 ]
Bersini, Simone [2 ]
Moretti, Matteo [2 ,6 ,7 ,8 ]
机构
[1] Politecn Milan, Dept Elect Informat & Bioengn, I-20133 Milan, Italy
[2] IRCCS Ist Ortoped Galeazzi, Cell & Tissue Engn Lab, I-20161 Milan, Italy
[3] Univ Milano Bicocca, PhD Sch Life Sci, Dept Biosci & Biotechnol, I-20126 Milan, Italy
[4] Univ Basel, Univ Basel Hosp, Dept Surg, CH-4065 Basel, Switzerland
[5] Univ Basel, Univ Basel Hosp, Dept Biomed, CH-4065 Basel, Switzerland
[6] Ente Osped Cantonale, Regenerat Med Technol Lab, CH-6900 Lugano, Switzerland
[7] Swiss Inst Regenerat Med, CH-6900 Lugano, Switzerland
[8] Cardioctr Ticino, CH-6900 Lugano, Switzerland
来源
MOLECULES | 2016年 / 21卷 / 09期
关键词
microfluidic; in vitro 3D model; skeletal muscle; cardiac muscle; heart; organ-on-a-chip; electrical stimulation; mechanical stimulation; IN-VITRO MODEL; ELECTRICAL-STIMULATION; OPTOGENETIC CONTROL; HEART-MUSCLE; CELL; PLATFORM; CARDIOMYOCYTES; CHIP; MYOCYTES; SYSTEMS;
D O I
10.3390/molecules21091128
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the last few years microfluidics and microfabrication technique principles have been extensively exploited for biomedical applications. In this framework, organs-on-a-chip represent promising tools to reproduce key features of functional tissue units within microscale culture chambers. These systems offer the possibility to investigate the effects of biochemical, mechanical, and electrical stimulations, which are usually applied to enhance the functionality of the engineered tissues. Since the functionality of muscle tissues relies on the 3D organization and on the perfect coupling between electrochemical stimulation and mechanical contraction, great efforts have been devoted to generate biomimetic skeletal and cardiac systems to allow high-throughput pathophysiological studies and drug screening. This review critically analyzes microfluidic platforms that were designed for skeletal and cardiac muscle tissue engineering. Our aim is to highlight which specific features of the engineered systems promoted a typical reorganization of the engineered construct and to discuss how promising design solutions exploited for skeletal muscle models could be applied to improve cardiac tissue models and vice versa.
引用
收藏
页数:21
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