Author
Listed:
- Alessia Urzi
(Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC))
- Ines Lahmann
(Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC))
- Lan Vi N. Nguyen
(Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC))
- Benjamin R. Rost
(German Center for Neurodegenerative Diseases (DZNE))
- Angélica García-Pérez
(Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC))
- Noemie Lelievre
(Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC))
- Megan E. Merritt-Garza
(Emory University School of Medicine)
- Han C. Phan
(University of Alabama)
- Gary J. Bassell
(Emory University School of Medicine)
- Wilfried Rossoll
(Mayo Clinic
Mayo Clinic)
- Sebastian Diecke
(Technology Platform Pluripotent Stem Cells)
- Severine Kunz
(Technology Platform Electron Microscopy)
- Dietmar Schmitz
(German Center for Neurodegenerative Diseases (DZNE)
Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin)
- Mina Gouti
(Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC))
Abstract
The complex neuromuscular network that controls body movements is the target of severe diseases that result in paralysis and death. Here, we report the development of a robust and efficient self-organizing neuromuscular junction (soNMJ) model from human pluripotent stem cells that can be maintained long-term in simple adherent conditions. The timely application of specific patterning signals instructs the simultaneous development and differentiation of position-specific brachial spinal neurons, skeletal muscles, and terminal Schwann cells. High-content imaging reveals self-organized bundles of aligned muscle fibers surrounded by innervating motor neurons that form functional neuromuscular junctions. Optogenetic activation and pharmacological interventions show that the spinal neurons actively instruct the synchronous skeletal muscle contraction. The generation of a soNMJ model from spinal muscular atrophy patient-specific iPSCs reveals that the number of NMJs and muscle contraction is severely affected, resembling the patient’s pathology. In the future, the soNMJ model could be used for high-throughput studies in disease modeling and drug development. Thus, this model will allow us to address unmet needs in the neuromuscular disease field.
Suggested Citation
Alessia Urzi & Ines Lahmann & Lan Vi N. Nguyen & Benjamin R. Rost & Angélica García-Pérez & Noemie Lelievre & Megan E. Merritt-Garza & Han C. Phan & Gary J. Bassell & Wilfried Rossoll & Sebastian Diec, 2023.
"Efficient generation of a self-organizing neuromuscular junction model from human pluripotent stem cells,"
Nature Communications, Nature, vol. 14(1), pages 1-15, December.
Handle:
RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43781-3
DOI: 10.1038/s41467-023-43781-3
Download full text from publisher
References listed on IDEAS
- Jeremy S. Dasen & Jeh-Ping Liu & Thomas M. Jessell, 2003.
"Motor neuron columnar fate imposed by sequential phases of Hox-c activity,"
Nature, Nature, vol. 425(6961), pages 926-933, October.
- Lingjun Rao & Ying Qian & Alastair Khodabukus & Thomas Ribar & Nenad Bursac, 2018.
"Engineering human pluripotent stem cells into a functional skeletal muscle tissue,"
Nature Communications, Nature, vol. 9(1), pages 1-12, December.
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