Excitatory neurons of the cerebral cortex are generated prenatally from a diverse group of neural precursors, some of which have only been identified recently. Radial glia stem cells (RGCs) generate neurons directly and at least three separate lineages of Intermediate Neural Precursor Cells (IPCs), which are themselves produced from RGC, also produce neurons. Intriguingly, neurons within each cortical lamina are derived from these different parent cells. The reason why the neocortex requires so many individual precursor cell types, and whether the diverse ancestry of neurons within each layer plays a functional role in neocortical circuitry, has not been established. The numbers of IPCs are thought to be abnormal in several developmental disabilities, including Fragile X and Down's syndromes. In this project, we identify specific lineages of neocortical pyramidal neurons with novel genetic fate mapping tools and determine their structural, functional and connectional characteristics with patch clamp electrophysiology and high resolution 3D imaging. Our preliminary data indicate that neurons from individual precursor lineages, even within the same lamina, are imparted with specific functional properties and that the multiple IPC groups therefore directly underlie neuron and circuit complexity in the neocortex. Morphological and electrophysiological parameters will be quantitatively examined using a multidisciplinary approach and a two-laboratory collaboration.

Public Health Relevance

The complex circuitry of the brain is formed by neurons which are born from many distinct precursor cells during development, but whether the diverse origins of these neurons leads to functional differences has not been determined. Changes in neural precursor cells have been found in several developmental disorders causing cognitive disability. Thus, understanding how proper circuits are formed will lead to advances in diagnosis and treatment. We have developed molecular techniques which enable simultaneous tracking and functional testing of multiple neuron lineages in vivo. These studies address how circuit complexity is influenced by the diverse population of neural precursor cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21NS089340-02
Application #
8926479
Study Section
Neurotransporters, Receptors, and Calcium Signaling Study Section (NTRC)
Program Officer
Riddle, Robert D
Project Start
2014-09-15
Project End
2016-08-31
Budget Start
2015-09-01
Budget End
2016-08-31
Support Year
2
Fiscal Year
2015
Total Cost
$204,625
Indirect Cost
$79,625
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; Medalla, Maria; Guillamon-Vivancos, Teresa et al. (2015) Neural precursor lineages specify distinct neocortical pyramidal neuron types. J Neurosci 35:6142-52