Biomimetic engineered muscle with capacity for vascular integration and functional maturation in vivo

被引:190
作者
Juhas, Mark [1 ]
Engelmayr, George C., Jr. [1 ]
Fontanella, Andrew N. [1 ]
Palmer, Gregory M. [2 ]
Bursac, Nenad [1 ]
机构
[1] Duke Univ, Dept Biomed Engn, Durham, NC 27708 USA
[2] Duke Univ, Sch Med, Dept Radiat Oncol, Durham, NC 27710 USA
基金
美国国家科学基金会;
关键词
tissue engineering; contractile force; self-repair; angiogenesis; window chamber; SKELETAL-MUSCLE; SATELLITE CELLS; SELF-RENEWAL; STEM-CELLS; TISSUE; REGENERATION; VITRO; CONSTRUCTS; INJURY; MICE;
D O I
10.1073/pnas.1402723111
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Tissue-engineered skeletal muscle can serve as a physiological model of natural muscle and a potential therapeutic vehicle for rapid repair of severe muscle loss and injury. Here, we describe a platform for engineering and testing highly functional biomimetic muscle tissues with a resident satellite cell niche and capacity for robust myogenesis and self-regeneration in vitro. Using a mouse dorsal window implantation model and transduction with fluorescent intracellular calcium indicator, GCaMP3, we nondestructively monitored, in real time, vascular integration and the functional state of engineered muscle in vivo. During a 2-wk period, implanted engineered muscle exhibited a steady ingrowth of blood-perfused microvasculature along with an increase in amplitude of calcium transients and force of contraction. We also demonstrated superior structural organization, vascularization, and contractile function of fully differentiated vs. undifferentiated engineered muscle implants. The described in vitro and in vivo models of biomimetic engineered muscle represent enabling technology for novel studies of skeletal muscle function and regeneration.
引用
收藏
页码:5508 / 5513
页数:6
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