Corey Harwell, PhD

We are interested in understanding how the extensive morphological, molecular and functional diversity of neural cell types is achieved during development of the central nervous system. We focus our studies on the forebrain, with particular attention to the cortex and the septal nuclei of the basal forebrain. Our long-term goal is to understand how genetic and epigenetic programs associated with a progenitor cells spatial and temporal identity dictates their fate choice. We are also interested in understanding how these diverse groups of neurons and glia coordinate to assemble the precise circuitry of the mammalian forebrain.

Project 1 
Genetic and epigenetic regulation of neural cell fate specification. 
Radial glial cells serve as the primary neural progenitors of the central nervous system. Radial glial cells transition through a series of competence states as they undergo multiple divisions to produce clonal lineages composed of diverse neural cell types. We are interested in understanding how progenitors ‘know’ when to switch from producing one neural cell type to another. We are also interested in understanding how epigenetic modifications in progenitors to provide instructions to their neuronal progeny important for fate specification.

 Project 2 
Developmental diversity of spatial and temporal lineages in the septum. 
Septal nuclei in the basal forebrain have critical roles in regulating emotional and motivational states. The septum is composed of a diverse array of GABAergic, cholinergic and glutamatergic projection neurons. We know very little about the specific functions of these diverse septal neuron types and even less about the developmental mechanisms that create this diversity. We are interested in understanding the molecular programs involved in specifying these distinct projection neuron subgroups, and how their circuitry and functional properties regulates innate behaviors. 

Project 3 
Neuron-glia crosstalk during circuit assembly 
The nervous system is comprised of two main cell types, neurons and glia. Neurons connected through chemical and electrical synapses form complex networks in the brain. Glial cells have a broad range of functions that influence the formation and activity of neuronal networks. Astrocytes are the most numerous and diverse glial cell in the mammalian brain. They have crucial roles in regulatiing synapse formation and pruning. The mechanism by which astrocytes  and neurons communicate and coordinate with each other is not well understood. We are interested in uncovering the secreted signals that neurons and astrocytes use to communicate, and the specific ‘messages’ encoded by those factors. 
 

Lab members 
 
Miguel Turrero Garcia, Ph.D. 
Yajun Xie, Ph.D. 
Manal Adam, Ph.D. 
Yuqi Ren, Ph.D. 
Khalida Sabeur, Ph.D. 
Christopher Reid 
Sarah Hanson 
Sandra Chang 
 
Academic community service and committee membership:
Neuroscience Program DEI Committee, Advancement & Promotions Committee Neurology Department