On-chip 3D neuromuscular model for drug screening and precision medicine in neuromuscular disease

被引:98
作者
Osaki, Tatsuya [1 ]
Uzel, Sebastien G. M. [2 ,3 ]
Kamm, Roger D. [1 ,4 ,5 ]
机构
[1] MIT, Dept Mech Engn, Cambridge, MA 02139 USA
[2] Harvard Univ, Wyss Inst Biol Inspired Engn, Cambridge, MA 02138 USA
[3] Harvard Univ, John A Paulson Sch Engn & Appl Sci, Cambridge, MA 02138 USA
[4] MIT, Dept Biol Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[5] Koch Inst Integrat Canc Res, Cambridge, MA 02142 USA
基金
美国国家科学基金会; 日本学术振兴会;
关键词
MOUSE MODEL; JUNCTION; CULTURE; ALS; ELECTROPHYSIOLOGY; QUANTIFICATION; MICROFLUIDICS; NEUROSCIENCE; PLATFORM; NEURONS;
D O I
10.1038/s41596-019-0248-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This protocol describes the design, fabrication and use of a 3D physiological and pathophysiological motor unit model consisting of motor neurons coupled to skeletal muscles interacting via the neuromuscular junction (NMJ) within a microfluidic device. This model facilitates imaging and quantitative functional assessment. The 'NMJ chip' enables real-time, live imaging of axonal outgrowth, NMJ formation and muscle maturation, as well as synchronization of motor neuron activity and muscle contraction under optogenetic control for the study of normal physiological events. The proposed protocol takes similar to 2-3 months to be implemented. Pathological behaviors associated with various neuromuscular diseases, such as regression of motor neuron axons, motor neuron death, and muscle degradation and atrophy can also be recapitulated in this system. Disease models can be created by the use of patient-derived induced pluripotent stem cells to generate both the motor neurons and skeletal muscle cells used. This is demonstrated by the use of cells from a patient with sporadic amyotrophic lateral sclerosis but can be applied more generally to models of neuromuscular disease, such as spinal muscular atrophy, NMJ disorder and muscular dystrophy. Models such as this hold considerable potential for applications in precision medicine, drug screening and disease risk assessment.
引用
收藏
页码:421 / 449
页数:29
相关论文
共 59 条
[1]  
Afshar M. E., 2019, 96 WELL CULTURE PLAT, DOI [10.1101/562819v1, DOI 10.1101/562819V1]
[2]   Applications of Light-Sheet Microscopy in Microdevices [J].
Albert-Smet, Ignacio ;
Marcos-Vidal, Asier ;
Jose Vaquero, Juan ;
Desco, Manuel ;
Munoz-Barrutia, Arrate ;
Ripoll, Jorge .
FRONTIERS IN NEUROANATOMY, 2019, 13
[3]   Oxidative stress in neurodegeneration: cause or consequence? [J].
Andersen, JK .
NATURE MEDICINE, 2004, 10 (07) :S18-S25
[4]   A 3D culture model of innervated human skeletal muscle enables studies of the adult neuromuscular junction [J].
Bakooshli, Mohsen Afshar ;
Lippmann, Ethan S. ;
Mulcahy, Ben ;
Iyer, Nisha ;
Nguyen, Christine T. ;
Tung, Kayee ;
Stewart, Bryan A. ;
van den Dorpel, Hubrecht ;
Fuehrmann, Tobias ;
Shoichet, Molly ;
Bigot, Anne ;
Pegoraro, Elena ;
Ahn, Henry ;
Ginsberg, Howard ;
Zhen, Mei ;
Ashton, Randolph Scott ;
Gilbert, Penney M. .
ELIFE, 2019, 8
[5]   Hit and lead generation:: Beyond high-throughput screening [J].
Bleicher, KH ;
Böhm, HJ ;
Müller, K ;
Alanine, AI .
NATURE REVIEWS DRUG DISCOVERY, 2003, 2 (05) :369-378
[6]  
Brooks BR, 1996, NEUROLOGY, V47, pS71, DOI 10.1212/WNL.47.4_Suppl_2.71S
[7]   The relationship between four GWAS-identified loci in Alzheimer's disease and the risk of Parkinson's disease, amyotrophic lateral sclerosis, and multiple system atrophy [J].
Chen, Yongping ;
Cao, Bei ;
Chen, Xueping ;
Ou, Ruwei ;
Wei, Qianqian ;
Zhao, Bi ;
Wu, Ying ;
Yuan, Lixing ;
Shang, Hui-Fang .
NEUROSCIENCE LETTERS, 2018, 686 :205-210
[8]   Industrial choices for protein production by large-scale cell culture [J].
Chu, L ;
Robinson, DK .
CURRENT OPINION IN BIOTECHNOLOGY, 2001, 12 (02) :180-187
[9]   Multiple sclerosis [J].
Compston, Alastair ;
Coles, Alasdair .
LANCET, 2008, 372 (9648) :1502-1517
[10]   High-content screening of primary neurons: ready for prime time [J].
Daub, Aaron ;
Sharma, Punita ;
Finkbeiner, Steven .
CURRENT OPINION IN NEUROBIOLOGY, 2009, 19 (05) :537-543