Modeling Huntington's disease with induced pluripotent stem cells.

Mol Cell Neurosci

Gladstone Institute of Neurological Disease, 1650 Owens Street, San Francisco, CA 94158, United States. Electronic address:

Published: September 2013

Huntington's disease (HD) causes severe motor dysfunction, behavioral abnormalities, cognitive impairment and death. Investigations into its molecular pathology have primarily relied on murine tissues; however, the recent discovery of induced pluripotent stem cells (iPSCs) has opened new possibilities to model neurodegenerative disease using cells derived directly from patients, and therefore may provide a human-cell-based platform for unique insights into the pathogenesis of HD. Here, we will examine the practical implementation of iPSCs to study HD, such as approaches to differentiate embryonic stem cells (ESCs) or iPSCs into medium spiny neurons, the cell type most susceptible in HD. We will explore the HD-related phenotypes identified in iPSCs and ESCs and review how brain development and neurogenesis may actually be altered early, before the onset of HD symptoms, which could inform the search for drugs that delay disease onset. Finally, we will speculate on the exciting possibility that ESCs or iPSCs might be used as therapeutics to restore or replace dying neurons in HD brains.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3791169PMC
http://dx.doi.org/10.1016/j.mcn.2013.02.005DOI Listing

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