Three-dimensionally printed biological machines powered by skeletal muscle

被引:366
作者
Cvetkovic, Caroline [1 ,2 ]
Raman, Ritu [2 ,3 ]
Chan, Vincent [1 ,2 ,4 ]
Williams, Brian J. [2 ,3 ]
Tolish, Madeline [5 ]
Bajaj, Piyush [1 ,2 ]
Sakar, Mahmut Selman [4 ]
Asada, H. Harry [4 ]
Saif, M. Taher A. [2 ,3 ]
Bashir, Rashid [1 ,2 ]
机构
[1] Univ Illinois, Dept Bioengn, Urbana, IL 61801 USA
[2] Univ Illinois, Micro & Nanotechnol Lab, Urbana, IL 61801 USA
[3] Univ Illinois, Dept Mech Sci & Engn, Urbana, IL 61801 USA
[4] MIT, Dept Mech Engn, Cambridge, MA 02139 USA
[5] Vanderbilt Univ, Dept Biomed Engn, Nashville, TN 37325 USA
基金
美国国家科学基金会;
关键词
bioactuator; stereolithography; ELECTRICAL-STIMULATION; FORCE GENERATION; TISSUE; FABRICATION; EXPRESSION; INSULIN; STEREOLITHOGRAPHY; DIFFERENTIATION; EXCITABILITY; CHALLENGES;
D O I
10.1073/pnas.1401577111
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
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Combining biological components, such as cells and tissues, with soft robotics can enable the fabrication of biological machines with the ability to sense, process signals, and produce force. An intuitive demonstration of a biological machine is one that can produce motion in response to controllable external signaling. Whereas cardiac cell-driven biological actuators have been demonstrated, the requirements of these machines to respond to stimuli and exhibit controlled movement merit the use of skeletal muscle, the primary generator of actuation in animals, as a contractile power source. Here, we report the development of 3D printed hydrogel "bio-bots" with an asymmetric physical design and powered by the actuation of an engineered mammalian skeletal muscle strip to result in net locomotion of the bio-bot. Geometric design and material properties of the hydrogel bio-bots were optimized using stereolithographic 3D printing, and the effect of collagen I and fibrin extracellular matrix proteins and insulin-like growth factor 1 on the force production of engineered skeletal muscle was characterized. Electrical stimulation triggered contraction of cells in the muscle strip and net locomotion of the bio-bot with a maximum velocity of similar to 156 m s(-1), which is over 1.5 body lengths per min. Modeling and simulation were used to understand both the effect of different design parameters on the bio-bot and the mechanism of motion. This demonstration advances the goal of realizing forward-engineered integrated cellular machines and systems, which can have a myriad array of applications in drug screening, programmable tissue engineering, drug delivery, and biomimetic machine design.
引用
收藏
页码:10125 / 10130
页数:6
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