Gordon Fishell, PhD

Gordon FishellProfessor and Coordinator of the Smilow
Neuroscience Program
Ph.D., 1989 University of Toronto

Smilow Neuroscience Program
New York University School of Medicine
522 First Ave. SRB 311
New York, NY 10016
Tel: (212) 263-7691
Fax: (212) 263-2248
E-mail: fisheg01@nyumc.org
Lab Website: http://www.med.nyu.edu/fishelllab/

Research Theme(s): Cell Migration, Developmental Immunology, Segmentation and Pattern Formation, Stem Cell Biology
Keywords: Neural progenitor, Genetics, Forebrain, Epilepsy, Autism Spectral Disease, Cortical Interneurons

Research Summary:

The Fishell laboratory uses mice to study cortical microcircuits. In particular we are interested in cortical interneurons, which are generated within the medial and caudal ganglionic eminences. We wish to understand the logic of the combinatorial codes by which different classes of cortical interneurons are generated and wish to relate this code to their emergent properties including: their synaptic connectivity, intrinsic firing properties and their unique morphologies.

Understanding the embryonic molecular and genetic origins of cortical interneurons promises to open the way for understanding how different functional classes of interneurons are generated and the logic by which each subclass contribute to the assembly of cortical microcircuits. Our goals in this regard are three fold and together they comprise the breadth of interests of the Fishell laboratory.

  1. Using inducible genetic fate mapping and conditional loss of function analysis, in combination with genome-wide microarray analysis of cortical interneurons to study how developmental gene expression leads to the emergence of cortical interneurons with distinct functional properties.
  2. To use the precision achieved through genetic methods to understand the “rules” by which specific subclasses of cortical interneurons integrate into the postnatal cortex.
  3. Beyond understanding the logic by which cortical microcircuits develop, we wish to develop genetic tools by which specific cortical interneuronal populations can be manipulated to a) trace their synaptic circuitry b) visualize, induce or suppress their activity in vivo c) explore the cellular mechanisms by which they maintain their unique architectures.

Through these multifaceted methods, a picture of the logic by which cortical microcircuits are established is beginning to emerge. At present we are examining how the loss of developmental genes affects the gene expression patterns, electrophysiological properties and fine cytoarchitecture of the mature neurons. Through this effort we are beginning to connect embryonic gene expression to mature neuronal phenotypes.

 Research is supported by the NINDS, NIMH, NYSTEM, The Simons Foundation. 


Selected Publications: