Transcriptomic analysis of loss of Gli1 in neural stem cells responding to demyelination in the mouse brain

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Jayshree Samanta
Hernandez Moura Silva
Juan J. Lafaille
James L. Salzer
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[1] New York University School of Medicine,Department of Neuroscience and Physiology, Neuroscience Institute
[2] New York University School of Medicine,The Kimmel Center for Biology and Medicine of the Skirball Institute
[3] University of Wisconsin-Madison,Stem Cell and Regenerative Medicine Center, Department of Comparative Biosciences, School of Veterinary Medicine
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In the adult mammalian brain, Gli1 expressing neural stem cells reside in the subventricular zone and their progeny are recruited to sites of demyelination in the white matter where they generate new oligodendrocytes, the myelin forming cells. Remarkably, genetic loss or pharmacologic inhibition of Gli1 enhances the efficacy of remyelination by these neural stem cells. To understand the molecular mechanisms involved, we performed a transcriptomic analysis of this Gli1-pool of neural stem cells. We compared murine NSCs with either intact or deficient Gli1 expression from adult mice on a control diet or on a cuprizone diet which induces widespread demyelination. These data will be a valuable resource for identifying therapeutic targets for enhancing remyelination in demyelinating diseases like multiple sclerosis.
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