Corey Harwell

  • Latest publications

    Baizabal, J. M., Mistry, M., Garcia, M. T., Gomez, N., Olukoya, O., Tran, D., Johnson, M. B., Walsh, C. A., and Harwell, C. C. (2018) The Epigenetic State of PRDM16-Regulated Enhancers in Radial Glia Controls Cortical Neuron Position, Neuron.

    Turrero Garcia, M., and Harwell, C. C. (2017) Radial glia in the ventral telencephalon, FEBS letters 591, 3942-3959.

    Turrero Garcia, M., Mazzola, E., and Harwell, C. C. (2016) Lineage Relationships Do Not Drive MGE/PoA-Derived Interneuron Clustering in the Brain, Neuron 92, 52-58.

    Harwell, C. C., Fuentealba, L. C., Gonzalez-Cerrillo, A., Parker, P. R., Gertz, C. C., Mazzola, E., Garcia, M. T., Alvarez-Buylla, A., Cepko, C. L., and Kriegstein, A. R. (2015) Wide Dispersion and Diversity of Clonally Related Inhibitory Interneurons, Neuron 87, 999-1007.

    Harwell, C. C., Parker, P. R., Gee, S. M., Okada, A., McConnell, S. K., Kreitzer, A. C., and Kriegstein, A. R. (2012) Sonic hedgehog expression in corticofugal projection neurons directs cortical microcircuit formation, Neuron 73, 1116-1126.

  • Prizes and Awards

    NINDS Faculty Career Development Award

    Giovanni Armenise Harvard Foundation Junior Faculty Grant, Department of Neurobiology, “Temporal Specification of Circuits Regulating Anxiety-Related Behaviors”, 2018

Who he is

Corey is a native of Louisville, Kentucky. He obtained his B.S. in Chemistry from Tennessee State University in 2000 and his PhD in Neuroscience from MIT in 2006. After working as a postdoctoral fellow at University of California, San Francisco with Arnold Kriegstein, he joined the Harvard Medical School Department of Neurobiology in 2013.

What he does

The Harwell Lab is focused on understanding how lineage of neural cell types influences their mature function. His lab follows specific subgroups of neural progenitors through developmental time to understand the genetic and epigenetic programs that determine their ultimate fate. This work requires a multidisciplinary approach utilizing molecular genetics, molecular biology, and neural circuit mapping techniques to analyze the function of temporally defined subgroups of neurons in the developing brain. Together these diverse approaches provide a comprehensive picture of the molecular specification of distinct neuronal cell types and their functional relevance within circuits of the brain.

Current goals of the lab are to understand:

  1. The molecular and cellular diversity of forebrain progenitors
  2. Genetic and epigenetic regulation of cell fate and neuronal diversity
  3. Molecular mechanisms by which forebrain neurons are assembled into functional circuits

News from the Lab

The epigenetic landscape of neural stem cells is dynamically remodeled during neurogenesis. However, it is not understood how chromatin modifications in neural stem cells instruct the formation of complex structures in the brain. A recent report from the Harwell Lab showed that the histone methytransferase PRDM16 is required in neural stem cells to regulate lineage-autonomous and stage-specific gene expression programs that control the growth and organization of circuits in the brain. PRDM16 functions to regulate the epigenetic state of noncoding regions of the genome known as enhancers that control the expression of genes involved in neuron production and migration. These finding provide new insights into how epigenetic control of transcriptional enhancers in neural stem cells determines the organization of the mammalian brain.