Modeling ALS with motor neurons derived from human induced pluripotent stem cells.
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Abstract | Directing the differentiation of induced pluripotent stem cells into motor neurons has allowed investigators to develop new models of amyotrophic lateral sclerosis (ALS). However, techniques vary between laboratories and the cells do not appear to mature into fully functional adult motor neurons. Here we discuss common developmental principles of both lower and upper motor neuron development that have led to specific derivation techniques. We then suggest how these motor neurons may be matured further either through direct expression or administration of specific factors or coculture approaches with other tissues. Ultimately, through a greater understanding of motor neuron biology, it will be possible to establish more reliable models of ALS. These in turn will have a greater chance of validating new drugs that may be effective for the disease. |
Year of Publication | 2016
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Journal | Nat Neurosci
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Volume | 19
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Issue | 4
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Pages | 542-53
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Date Published | 2016 Apr
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ISSN | 1546-1726
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DOI | 10.1038/nn.4273
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PubMed ID | 27021939
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PubMed Central ID | PMC5015775
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Grant list | R01 NS049553 / NS / NINDS NIH HHS / United States
R37NS041590 / NS / NINDS NIH HHS / United States
R37 NS041590 / NS / NINDS NIH HHS / United States
R01 NS041590 / NS / NINDS NIH HHS / United States
R01NS045523 / NS / NINDS NIH HHS / United States
R01NS075672 / NS / NINDS NIH HHS / United States
P30 DK063491 / DK / NIDDK NIH HHS / United States
R01 NS045523 / NS / NINDS NIH HHS / United States
R01NS049553 / NS / NINDS NIH HHS / United States
R01 NS075672 / NS / NINDS NIH HHS / United States
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