Cited by 163Nerve injury and regenerationNeuroscience and Neural EngineeringMuscle Physiology and Disorders

The DOI matches its Crossref record; 28 of the 28 references it cites were found in a registry or an index.

Optical Control of Muscle Function by Transplantation of Stem Cell–Derived Motor Neurons in Mice

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Abstract

Optogenetics Applied to Motorneuron Control: Nerves damaged by disease or injury do not always regenerate. In such cases, therapies involving transplanted stem cells show some promise. However, the new neurons derived from transplanted cells cannot communicate with the central control systems that would normally regulate movement. To avoid the need for such communication, in a proof-of-principle study, Bryson et al. (p. 94 ; see the Perspective by Iyer and Delp ) added optogenetic control to differentiation and transplantation of motor neurons. In the mouse, these engineered neurons were able to reestablish connections within a damaged sciatic nerve and, when activated by localized light stimulation, could drive muscle contractions.

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  1. 10.1227/00006123-198512000-00021 · DOI · Paper page

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Metadata

Authors
Bryson, J. B., Machado, C. B., Crossley, M., Stevenson, D., Bros-Facer, V., Burrone, J., Greensmith, L., & Lieberam, I.
Affiliations
  • UCL Queen Square Institute of Neurology (GB)
  • Guy's Hospital (GB)
  • Sobell Department of Motor Neuroscience and Movement Disorders, University College London (UCL) Institute of Neurology, London, UK.
Corresponding author
  • Machado, Carolina Barcellos
  • Crossley, Martin
  • Stevenson, Danielle
  • Greensmith, Linda
  • Lieberam, Ivo
Venue
Science
Published
2014-04-04
Volume
344
Issue
6179
Pages
94-97
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2055697048
Cited by
163
References
27
Citations by year
2026: 3 · 2025: 9 · 2024: 3 · 2023: 10 · 2022: 14 · 2021: 13 · 2020: 10 · 2019: 14 · 2018: 14 · 2017: 18 · 2016: 26 · 2015: 17 · 2014: 12
FWCI
11.13
Type
journal article
Language
en
Open access
Locations
  • Science (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
  • UCL Discovery (University College London) (acceptedVersion)
  • Research Portal (King's College London) (submittedVersion)
Funders
  • Wellcome Trust (095589)
  • Medical Research Council (MR/K000608/1)
  • Biotechnology and Biological Sciences Research Council (G1001234)
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neural Engineering
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
Keywords
optogenetics, channelrhodopsin-2, central nervous system injury, regenerative medicine
MeSH terms
Channelrhodopsins, Animals, Axons, Cell Line, Electric Stimulation, Female, Hindlimb, Isometric Contraction, Light, Mice, Inbred C57BL, Motor Neurons, Muscle Denervation, Nerve Regeneration, Sciatic Nerve, Transfection, Muscle, Skeletal, Muscle Fibers, Skeletal, Transgenes, Mice, Embryonic Stem Cells, Optogenetics

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