In vitro Neuromuscular Junction Induced from Human Induced Pluripotent Stem Cells.

The neuromuscular junction (NMJ) is a specialized synapse that transmits action potentials from the motor neuron to skeletal muscle for mechanical movement. The architecture of the NMJ structure influences the functions of the neuron, the muscle and the mutual interaction. Previous studies have reported many strategies by co-culturing the motor neurons and myotubes to generate NMJ in vitro with complex induction process and long culture period but have struggled to recapitulate mature NMJ morphology and function. Our in vitro NMJ induction system is constructed by differentiating human iPSC in a single culture dish. By switching the myogenic and neurogenic induction medium for induction, the resulting NMJ contained pre- and post- synaptic components, including motor neurons, skeletal muscle and Schwann cells in the one month culture. The functional assay of NMJ also showed that the myotubes contraction can be triggered by Ca++ then inhibited by curare, an acetylcholine receptor (AChR) inhibitor, in which the stimulating signal is transmitted through NMJ. This simple and robust approach successfully derived the complex structure of NMJ with functional connectivity. This in vitro human NMJ, with its integrated structures and function, has promising potential for studying pathological mechanisms and compound screening.

[1]  H. Sakurai,et al.  iPSC-derived functional human neuromuscular junctions model the pathophysiology of neuromuscular diseases. , 2019, JCI insight.

[2]  R. Mirsky,et al.  Schwann Cell Precursors; Multipotent Glial Cells in Embryonic Nerves , 2019, Front. Mol. Neurosci..

[3]  A. Furlan,et al.  Schwann cell precursor: a neural crest cell in disguise? , 2018, Developmental biology.

[4]  J. Hickman,et al.  Stem cell derived phenotypic human neuromuscular junction model for dose response evaluation of therapeutics. , 2018, Biomaterials.

[5]  D. Re,et al.  Limitations and Challenges in Modeling Diseases Involving Spinal Motor Neuron Degeneration in Vitro , 2018, Front. Cell. Neurosci..

[6]  C. Soeller,et al.  Cellular and Molecular Anatomy of the Human Neuromuscular Junction , 2017, Cell reports.

[7]  C. Slater The Structure of Human Neuromuscular Junctions: Some Unanswered Molecular Questions , 2017, International journal of molecular sciences.

[8]  Roger D. Kamm,et al.  Microfluidic device for the formation of optically excitable, three-dimensional, compartmentalized motor units , 2016, Science Advances.

[9]  E. Gomes,et al.  A system for studying mechanisms of neuromuscular junction development and maintenance , 2016, Development.

[10]  A. Weishaupt,et al.  Functional Connectivity under Optogenetic Control Allows Modeling of Human Neuromuscular Disease. , 2016, Cell stem cell.

[11]  E. Hedlund,et al.  Cross‐disease comparison of amyotrophic lateral sclerosis and spinal muscular atrophy reveals conservation of selective vulnerability but differential neuromuscular junction pathology , 2015, The Journal of comparative neurology.

[12]  K. Föhr,et al.  Formation and characterisation of neuromuscular junctions between hiPSC derived motoneurons and myotubes. , 2015, Stem cell research.

[13]  J. Takahashi,et al.  Modeling the Early Phenotype at the Neuromuscular Junction of Spinal Muscular Atrophy Using Patient-Derived iPSCs , 2015, Stem cell reports.

[14]  S. Corti,et al.  Motor neuron derivation from human embryonic and induced pluripotent stem cells: experimental approaches and clinical perspectives , 2014, Stem Cell Research & Therapy.

[15]  N. Fujii,et al.  Efficient and Reproducible Myogenic Differentiation from Human iPS Cells: Prospects for Modeling Miyoshi Myopathy In Vitro , 2013, PloS one.

[16]  K. Shigemoto,et al.  Muscle weakness and neuromuscular junctions in aging and disease , 2010, Geriatrics & gerontology international.

[17]  H. Weintraub,et al.  Expression of a single transfected cDNA converts fibroblasts to myoblasts , 1987, Cell.

[18]  A. Engel Congenital Myasthenic Syndromes , 1985, Journal of child neurology.

[19]  E. Reynolds THE USE OF LEAD CITRATE AT HIGH pH AS AN ELECTRON-OPAQUE STAIN IN ELECTRON MICROSCOPY , 1963, The Journal of cell biology.

[20]  J. Sanes,et al.  Development of the vertebrate neuromuscular junction. , 1999, Annual review of neuroscience.