Accelerated High-Yield Generation of Limb-Innervating Motor Neurons from Human Stem Cells
Human pluripotent stem cells are a promising source of differentiated cells for developmental studies, cell transplantation, disease modeling, and drug testing. However, their widespread use even for intensely studied cell types like spinal motor neurons is hindered by the long duration and low yiel...
Saved in:
Published in | The Journal of neuroscience Vol. 33; no. 2; pp. 574 - 586 |
---|---|
Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Society for Neuroscience
09.01.2013
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Human pluripotent stem cells are a promising source of differentiated cells for developmental studies, cell transplantation, disease modeling, and drug testing. However, their widespread use even for intensely studied cell types like spinal motor neurons is hindered by the long duration and low yields of existing protocols for
in vitro
differentiation and by the molecular heterogeneity of the populations generated. We report a combination of small molecules that within 3 weeks induce motor neurons at up to 50% abundance and with defined subtype identities of relevance to neurodegenerative disease. Despite their accelerated differentiation, motor neurons expressed combinations of HB9, ISL1, and column-specific markers that mirror those observed
in vivo
in human embryonic spinal cord. They also exhibited spontaneous and induced activity, and projected axons toward muscles when grafted into developing chick spinal cord. Strikingly, this novel protocol preferentially generates motor neurons expressing markers of limb-innervating lateral motor column motor neurons (FOXP1
+
/LHX3
−
). Access to high-yield cultures of human limb-innervating motor neuron subtypes will facilitate in-depth study of motor neuron subtype-specific properties, disease modeling, and development of large-scale cell-based screening assays. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 M.W. Amoroso's present address: Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138. M.W.A. and G.F.C. contributed equally to this work. Author contributions: M.W.A., C.E.H., and H.W. designed research; M.W.A., G.F.C., D.J.W., S.O., and H.W. performed research; G.F.C., M.A.C., A.R.D., L.R., D.H.O., and T.M. contributed unpublished reagents/analytic tools; M.W.A., D.J.W., and H.W. analyzed data; M.W.A., C.E.H., and H.W. wrote the paper. |
ISSN: | 0270-6474 1529-2401 1529-2401 |
DOI: | 10.1523/JNEUROSCI.0906-12.2013 |