Department of Biomedical Engineering, Duke University, Durham, NC, USA.
Department of Biomedical Engineering, Duke University, Durham, NC, USA.
Biomaterials. 2019 Nov;221:119416. doi: 10.1016/j.biomaterials.2019.119416. Epub 2019 Aug 8.
Skeletal muscle is the largest organ of human body with several important roles in everyday movement and metabolic homeostasis. The limited ability of small animal models of muscle disease to accurately predict drug efficacy and toxicity in humans has prompted the development in vitro models of human skeletal muscle that fatefully recapitulate cell and tissue level functions and drug responses. We first review methods for development of three-dimensional engineered muscle tissues and organ-on-a-chip microphysiological systems and discuss their potential utility in drug discovery research and development of new regenerative therapies. Furthermore, we describe strategies to increase the functional maturation of engineered muscle, and motivate the importance of incorporating multiple tissue types on the same chip to model organ cross-talk and generate more predictive drug development platforms. Finally, we review the ability of available in vitro systems to model diseases such as type II diabetes, Duchenne muscular dystrophy, Pompe disease, and dysferlinopathy.
骨骼肌是人体最大的器官,在日常运动和代谢稳态中具有重要作用。肌肉疾病小动物模型在准确预测药物疗效和毒性方面的能力有限,促使人们开发了能够在细胞和组织水平上重现功能和药物反应的人类骨骼肌体外模型。我们首先回顾了三维工程肌肉组织和器官芯片微生理系统的开发方法,并讨论了它们在药物发现研究和新型再生治疗方法开发中的潜在应用。此外,我们还描述了增加工程肌肉功能成熟度的策略,并强调了在同一芯片上整合多种组织类型以模拟器官串扰和生成更具预测性的药物开发平台的重要性。最后,我们回顾了现有的体外系统在模拟 II 型糖尿病、杜氏肌营养不良症、庞贝病和 dysferlinopathy 等疾病方面的能力。