Mutant Ataxin-1 Inhibits Neural Progenitor Cell Proliferation in SCA1
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Spinocerebellar ataxia type 1 (SCA1) is a dominantly inherited neurodegenerative disease caused by the expansion of a polyglutamine (Q) repeat tract in the protein ataxin-1 (ATXN1). Beginning as a cerebellar ataxic disorder, SCA1 progresses to involve the cerebral cortex, hippocampus, and brainstem. Using SCA1 knock-in mice that mirror the complexity of the human disease, we report a significant decrease in the capacity of adult neuronal progenitor cells (NPCs) to proliferate. Remarkably, a decrease in NPCs proliferation can be observed in vitro, outside the degenerative milieu of surrounding neurons or glia, demonstrating that mutant ATXN1 acting cell autonomously within progenitor cells interferes with their ability to proliferate. Our findings suggest that compromised adult neurogenesis contributes to the progressive pathology of the disease particularly in areas such as the hippocampus and cerebral cortex where stem cells provide neurotropic factors and participate in adult neurogenesis. These findings not only shed light on the biology of the disease but also have therapeutic implications in any future stem cell-based clinical trials.
KeywordsSpinocerebellar ataxia type 1 SCA1 Neurogenesis Proliferation
We thank the members of the Opal lab for their intellectual input. We thank Jessica Huang for her help with the histopathology and mouse genotyping. MC was supported by startup funds for the Institute for the Translational Neuroscience and Minnesota Medical Foundation, while PO received grant support from the US National Institutes of Health (1R01 NS062051 and 1R01NS082351).
Compliance with Ethical Standards
All animal experiments were performed in compliance with National Institutes of Health’s Guide for the Care and Use of Laboratory Animals and the Northwestern University Institutional Animal Care and Use Committee.
Conflict of Interest
The authors declare that they have no conflict of interest.
- 2.Opal P, Zoghbi HY. Diseases of the nervous system. Diseases of the Nervous System. 2002;II:1880-95.Google Scholar
- 12.Hu YS, Xu P, Pigino G, Brady ST, Larson J, Lazarov O. Complex environment experience rescues impaired neurogenesis, enhances synaptic plasticity, and attenuates neuropathology in familial Alzheimer’s disease-linked APPswe/PS1DeltaE9 mice. FASEB J Off Publ Fed Am Soc Exp Biol. 2010;24(6):1667–81.Google Scholar
- 28.Palmer TD, Markakis EA, Willhoite AR, Safar F, Gage FH. Fibroblast growth factor-2 activates a latent neurogenic program in neural stem cells from diverse regions of the adult CNS. J Neurosci Off J Soc Neurosci. 1999;19(19):8487–97.Google Scholar
- 30.Arsenijevic Y, Weiss S, Schneider B, Aebischer P. Insulin-like growth factor-I is necessary for neural stem cell proliferation and demonstrates distinct actions of epidermal growth factor and fibroblast growth factor-2. J Neurosci Off J Soc Neurosci. 2001;21(18):7194–202.Google Scholar