Two major goals of developmental neurobiology are to identify the germinal cells which form the central nervous system and to characterize the cellular and molecular mechanisms by which these cells generate the proper numbers and types of neurons and glial cells. Recently, retroviral and genetic studies in mice have demonstrated that radial glial cells (RGCs) contribute significantly to neocortical development by generating postmitotic neurons and then serving as the substrate for the migration of those daughter cells into the neocortical wall. Furthermore, RGCs are thought now to be the prenatal stem cell of the neocortex, and several groups have suggested that the neocortical ventricular zone (VZ) is composed solely of RGCs during embryonic neurogenesis. However, it remains unclear how a single VZ precursor cell type can generate the vast diversity of neocortical neurons. In addition, since multiple types of precursors have been found in the human and monkey VZ, whether this heterogeneity in the primate VZ represents evolutionary divergence of rodents and primates also remains a question. We have uncovered significant precursor diversity in the in vivo murine VZ. Through the use of multiple histological, genetic and ultrastructural techniques - many of which we innovated for this project - we now show that RGCs are joined by another type of resident VZ cell which we have named the short neural precursor cell (SNP). We demonstrate that RGCs and SNPs can be distinguished morphologically, molecularly, and with respect to proliferation kinetics and lineage potential. In addition, we have uncovered in vivo differences between classes of RGCs which suggest that not all RGCs are multipotent stem cells. Taken together, our published and Preliminary Data fundamentally alter our understanding of the composition of the mammalian VZ and clearly indicate that diversity in this germinal compartment is required for proper neocortical growth and function. This project will comprehensively test the overall hypothesis that the VZ becomes heterogeneous during embryonic development through diversification of a common VZ ancestor and that this complexity is necessary for proper neocortical growth.

Public Health Relevance

How the rich diversity in types of forebrain neurons is achieved during development is not well understood. In this project, we build upon our novel findings that different types of neural stem and progenitor cells exist in the embryonic brain and generate neurons via distinct mechanisms. Using in vivo molecular approaches to measure proliferation, neurogenesis and allocation of progeny from individual precursor groups, this study will uncover the spatiotemporal inter-relationships between these precursor cells and determine how interaction with the extracellular matrix in the germinal zone controls their neuronal output.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS051852-09
Application #
8208045
Study Section
Neurogenesis and Cell Fate Study Section (NCF)
Program Officer
Owens, David F
Project Start
2010-01-15
Project End
2014-12-31
Budget Start
2012-01-01
Budget End
2012-12-31
Support Year
9
Fiscal Year
2012
Total Cost
$350,718
Indirect Cost
$136,343
Name
Boston University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
604483045
City
Boston
State
MA
Country
United States
Zip Code
02118
Tyler, William A; Haydar, Tarik F (2013) Multiplex genetic fate mapping reveals a novel route of neocortical neurogenesis, which is altered in the Ts65Dn mouse model of Down syndrome. J Neurosci 33:5106-19
Hevner, Robert F; Haydar, Tarik F (2012) The (not necessarily) convoluted role of basal radial glia in cortical neurogenesis. Cereb Cortex 22:465-8
Stancik, Elizabeth K; Navarro-Quiroga, Ivan; Sellke, Robert et al. (2010) Heterogeneity in ventricular zone neural precursors contributes to neuronal fate diversity in the postnatal neocortex. J Neurosci 30:7028-36
Loulier, Karine; Lathia, Justin D; Marthiens, Veronique et al. (2009) beta1 integrin maintains integrity of the embryonic neocortical stem cell niche. PLoS Biol 7:e1000176
Gadea, Ana; Aguirre, Adan; Haydar, Tarik F et al. (2009) Endothelin-1 regulates oligodendrocyte development. J Neurosci 29:10047-62
Corbin, Joshua G; Gaiano, Nicholas; Juliano, Sharon L et al. (2008) Regulation of neural progenitor cell development in the nervous system. J Neurochem 106:2272-87
Corbin, Joshua G; Haydar, Tarik F (2007) Quantum dots for neuroscience research: new tools for old problems? Nanomedicine (Lond) 2:579-81
Navarro-Quiroga, Ivan; Chittajallu, Ramesh; Gallo, Vittorio et al. (2007) Long-term, selective gene expression in developing and adult hippocampal pyramidal neurons using focal in utero electroporation. J Neurosci 27:5007-11
Slotkin, Jonathan R; Chakrabarti, Lina; Dai, Hai Ning et al. (2007) In vivo quantum dot labeling of mammalian stem and progenitor cells. Dev Dyn 236:3393-401
Gal, Jonathan S; Morozov, Yury M; Ayoub, Albert E et al. (2006) Molecular and morphological heterogeneity of neural precursors in the mouse neocortical proliferative zones. J Neurosci 26:1045-56

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