There is great excitement in the field of stem cell biology because it may be possible to produce specific kinds of neural cells from ES cells, adult brain stem cells or even bone marrow stem cells. There is a considerable base of knowledge regarding the normal in vivo processes of neural fate induction, stabilization and specification. This important information needs to be expanded in molecular detail so that it can be applied to the goal of obtaining large numbers of stem/progenitor cells that will express only a neural fate when transplanted into damaged or congenitally deficit tissue. The proposed experiments will study the function of several transcription factors that are expressed early in the neural plate and which expand the neural ectoderm when over-expressed. Because these genes are downstream of neural inductive signaling and upstream of neural differentiation genes, we call them neural fate-stabilizing genes. We posit it is important to understand: (1) how neural fate-stabilizing genes function during the earliest steps of neural specification; (2) how these genes interact with each other to expand the embryonic neural stem cell population called the neural plate, and 3) how these genes direct embryonic neural stem cells down the desired differentiation pathways. Once the precise functions of these genes are understood in the embryo, we may be able to regulate their expression to expand neural stem cells, define various stages of neural stem cell specification and put this information to clinical use.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
3R01NS023158-20S2
Application #
7056936
Study Section
Molecular, Cellular and Developmental Neurosciences 2 (MDCN)
Program Officer
Leblanc, Gabrielle G
Project Start
1986-01-15
Project End
2007-05-31
Budget Start
2004-06-01
Budget End
2005-05-31
Support Year
20
Fiscal Year
2005
Total Cost
$13,704
Indirect Cost
Name
George Washington University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
043990498
City
Washington
State
DC
Country
United States
Zip Code
20052
Yan, Bo; Neilson, Karen M; Ranganathan, Ramya et al. (2015) Microarray identification of novel genes downstream of Six1, a critical factor in cranial placode, somite, and kidney development. Dev Dyn 244:181-210
Grant, Paaqua A; Yan, Bo; Johnson, Michael A et al. (2014) Novel animal pole-enriched maternal mRNAs are preferentially expressed in neural ectoderm. Dev Dyn 243:478-96
Lee, Hyun-Kyung; Lee, Hyun-Shik; Moody, Sally A (2014) Neural transcription factors: from embryos to neural stem cells. Mol Cells 37:705-12
Karpinski, Beverly A; Maynard, Thomas M; Fralish, Matthew S et al. (2014) Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome. Dis Model Mech 7:245-57
Moody, Sally A; Klein, Steven L; Karpinski, Beverley A et al. (2013) On becoming neural: what the embryo can tell us about differentiating neural stem cells. Am J Stem Cells 2:74-94
Yan, Bo; Neilson, Karen M; Moody, Sally A (2010) Microarray identification of novel downstream targets of FoxD4L1/D5, a critical component of the neural ectodermal transcriptional network. Dev Dyn 239:3467-80
Rogers, Crystal D; Moody, Sally A; Casey, Elena S (2009) Neural induction and factors that stabilize a neural fate. Birth Defects Res C Embryo Today 87:249-62
Yan, Bo; Neilson, Karen M; Moody, Sally A (2009) foxD5 plays a critical upstream role in regulating neural ectodermal fate and the onset of neural differentiation. Dev Biol 329:80-95
Yan, Bo; Neilson, Karen M; Moody, Sally A (2009) Notch signaling downstream of foxD5 promotes neural ectodermal transcription factors that inhibit neural differentiation. Dev Dyn 238:1358-65
Schlosser, Gerhard; Awtry, Tammy; Brugmann, Samantha A et al. (2008) Eya1 and Six1 promote neurogenesis in the cranial placodes in a SoxB1-dependent fashion. Dev Biol 320:199-214

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