Creating stem cell-derived neuromuscular junctions in vitro

被引:9
作者
Luttrell, Shawn M. [1 ,2 ]
Smith, Alec S. T. [2 ,3 ]
Mack, David L. [1 ,2 ,3 ]
机构
[1] Univ Washington, Dept Rehabil Med, Seattle, WA 98104 USA
[2] Univ Washington, Inst Stem Cell & Regenerat Med, Seattle, WA 98195 USA
[3] Univ Washington, Dept Physiol & Biophys, Seattle, WA 98195 USA
关键词
disease modeling; drug discovery; hiPSC; neuromuscular junction; NMJ; stem cells; AMYOTROPHIC-LATERAL-SCLEROSIS; TYROSINE KINASE MUSK; RAT SKELETAL-MUSCLE; ELECTRICAL-STIMULATION; MUSCULAR-DYSTROPHY; SCHWANN-CELLS; SPINAL-CORD; HUMAN-URINE; ACETYLCHOLINE-RECEPTORS; OPTOGENETIC CONTROL;
D O I
10.1002/mus.27360
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Recent development of novel therapies has improved mobility and quality of life for people suffering from inheritable neuromuscular disorders. Despite this progress, the majority of neuromuscular disorders are still incurable, in part due to a lack of predictive models of neuromuscular junction (NMJ) breakdown. Improvement of predictive models of a human NMJ would be transformative in terms of expanding our understanding of the mechanisms that underpin development, maintenance, and disease, and as a testbed with which to evaluate novel therapeutics. Induced pluripotent stem cells (iPSCs) are emerging as a clinically relevant and non-invasive cell source to create human NMJs to study synaptic development and maturation, as well as disease modeling and drug discovery. This review will highlight the recent advances and remaining challenges to generating an NMJ capable of eliciting contraction of stem cell-derived skeletal muscle in vitro. We explore the advantages and shortcomings of traditional NMJ culturing platforms, as well as the pioneering technologies and novel, biomimetic culturing systems currently in use to guide development and maturation of the neuromuscular synapse and extracellular microenvironment. Then, we will explore how this NMJ-in-a-dish can be used to study normal assembly and function of the efferent portion of the neuromuscular arc, and how neuromuscular disease-causing mutations disrupt structure, signaling, and function.
引用
收藏
页码:388 / 403
页数:16
相关论文
共 202 条
[1]   Efficient and rapid generation of induced pluripotent stem cells from human keratinocytes [J].
Aasen, Trond ;
Raya, Angel ;
Barrero, Maria J. ;
Garreta, Elena ;
Consiglio, Antonella ;
Gonzalez, Federico ;
Vassena, Rita ;
Bilic, Josipa ;
Pekarik, Vladimir ;
Tiscornia, Gustavo ;
Edel, Michael ;
Boue, Stephanie ;
Izpisua Belmonte, Juan Carlos .
NATURE BIOTECHNOLOGY, 2008, 26 (11) :1276-1284
[2]   Myogenic Differentiation of Muscular Dystrophy-Specific Induced Pluripotent Stem Cells for Use in Drug Discovery [J].
Abujarour, Ramzey ;
Bennett, Monica ;
Valamehr, Bahram ;
Lee, Tom Tong ;
Robinson, Megan ;
Robbins, David ;
Thuy Le ;
Lai, Kevin ;
Flynn, Peter .
STEM CELLS TRANSLATIONAL MEDICINE, 2014, 3 (02) :149-160
[3]   Cell surface receptors, nuclear receptors and ligands that regulate adipose tissue development [J].
Ailhaud, G .
CLINICA CHIMICA ACTA, 1999, 286 (1-2) :181-190
[4]  
Akhtar AZ, 2008, REV NEUROSCIENCE, V19, P47
[5]   Cell migration during morphogenesis [J].
Aman, Andy ;
Piotrowski, Tatjana .
DEVELOPMENTAL BIOLOGY, 2010, 341 (01) :20-33
[6]   Rapsyn is required for MuSK signaling and recruits synaptic components to a MuSK-containing scaffold [J].
Apel, ED ;
Glass, DJ ;
Moscoso, LM ;
Yancopoulos, GD ;
Sanes, JR .
NEURON, 1997, 18 (04) :623-635
[7]   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
[8]   Schwann Cells in Neuromuscular Junction Formation and Maintenance [J].
Barik, Arnab ;
Li, Lei ;
Sathyamurthy, Anupama ;
Xiong, Wen-Cheng ;
Mei, Lin .
JOURNAL OF NEUROSCIENCE, 2016, 36 (38) :9770-9781
[9]   Lessons from Darwin:: 21st century designs for clinical trials [J].
Becker, Robert E. .
CURRENT ALZHEIMER RESEARCH, 2007, 4 (04) :458-467
[10]   The Cytoplasmic Adaptor Protein Dok7 Activates the Receptor Tyrosine Kinase MuSK via Dimerization [J].
Bergamin, Elisa ;
Hallock, Peter T. ;
Burden, Steven J. ;
Hubbard, Stevan R. .
MOLECULAR CELL, 2010, 39 (01) :100-109