High Throughput Clonal Analyses of Gliogenesis in Neocortical and Paleocortical areas of the Mouse Brain

Project Summary
The brain critically relies on balanced production of neurons and glia during embryonic and early postnatal development.
Recently developed clonal lineage analysis has revealed the behavior of neural stem cells (NSCs) giving rise to neurons in
the cerebral cortex with unprecedented single-cell resolution. However, the clonal principles underlying the formation of
glia by NSCs remains unclear and has yet to be systematically investigated using these new technologies. Gliogenesis is
critical for proper neuronal functions and when disrupted, it can result in various neurological diseases. Reconstructing
how glia are generated from individual NSCs and organized in the cortex during development is essential to understand
the structure-function relationships and how they can be modulated by clone-specific factors. We have established a
genetically-based single-cell lineage tracing technique utilizing MADM (Mosaic Analysis with Double Markers) mice to
label NSCs in the developing cortex and begin to address this knowledge gap. Using this method we have found two
distinct populations of glia that occupy different territories of the cortex and its related structure the hippocampal
formation. The goal of the proposed research is to reconstruct, quantify, and mathematically model the behavior of
individually labeled NSCs in vivo in neocortical and paleocortical areas. This effort requires the development of
optimized imaging and analytical tools to ensure reliable and repeatable interpretation of quantitative data. To this end we
are developing light sheet microscopy and AI-based automated quantification methods to facilitate unbiased and precise
imaging and quantification of clonal data in the brain. Successful completion of our study will result in a comprehensive
map of single NSCs and their glial progeny in various cortical regions. Our approach will also establish a platform for
detailed quantitative and computational analysis of gliogenesis, glial diversity, and their potential for repair and
regenerative approaches in the cortex in the context of various neurological disorders and brain injury.
Potential for Broader Impact
Our approaches to understand how important constituents of the brain, the glial cells, develop have wide implications.
Disruption of glial development is the root of a range of pathological conditions in the brain. Therefore, understanding the
basic principles and cellular mechanisms that control gliogenesis is critical to appreciate not only how healthy
development may be controlled by systematic production of glial cells, but also how abnormalities in gliogenesis may
lead to devastating neurodevelopmental disorders and brain tumors.