Gord Fishell

Gord Fishell, Ph.D.

Professor of Neurobiology, Harvard Medical School

The Diverse Landscape of Inhibitory Interneurons

A century ago Ramon y Cajal dubbed the local short axon cells of the brain, the inhibitory interneurons, “the butterflies of the soul”. With characteristic insight, he inferred that these populations, which possess such enormous morphological diversity, would ultimately prove to have an equally impressive breadth of functional attributes. Recent studies have born out this prediction and shown that inhibitory interneurons are much more than simple gatekeepers of excitation. Depending on which interneuron subtype is recruited they are able to refine or unite brain activity in a startling multitude of ways.

The Fishell laboratory is focused on how this diversity is created. Understanding how this is accomplished during development remains one of the most daunting problems in biology. In particular, we wish to understand not only how the vast variety of inhibitory interneuron subtypes are generated but how they subsequently integrate into the bewildering array of neural circuits that are embedded in different brain structures.

Our working hypothesis is that this is achieved through a two-step process. The first involves genetic programs that in accordance with their birthdate create a finite number of cardinal interneuron subtypes. Following the tiling of these newly born cardinal subtypes across different brain structures, local cues act to create the definitive subtypes characteristic of the distinct cortical and subcortical areas. Importantly, as we have explored the molecular control of these events, it has become clear that perturbation of this process can result in a variety of brain dysfunctions including autism spectrum disorder, intellectual disability and schizophrenia. A new and growing interest in the laboratory is therefore aimed at seeing if better understanding of these developmental events can lead to the development of new treatments for these disorders.

Publications View
Radial glial cell line C6-R integrates preferentially in adult white matter and facilitates migration of coimplanted neurons in vivo.
Authors: Authors: Hormigo A, McCarthy M, Nothias JM, Hasegawa K, Huang W, Friedlander DR, Fischer I, Fishell G, Grumet M.
Exp Neurol
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Spatiotemporal selectivity of response to Notch1 signals in mammalian forebrain precursors.
Authors: Authors: Chambers CB, Peng Y, Nguyen H, Gaiano N, Fishell G, Nye JS.
Development
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Sonic hedgehog contributes to oligodendrocyte specification in the mammalian forebrain.
Authors: Authors: Nery S, Wichterle H, Fishell G.
Development
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The Gsh2 homeodomain gene controls multiple aspects of telencephalic development.
Authors: Authors: Corbin JG, Gaiano N, Machold RP, Langston A, Fishell G.
Development
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Radial glial identity is promoted by Notch1 signaling in the murine forebrain.
Authors: Authors: Gaiano N, Nye JS, Fishell G.
Neuron
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A method for rapid gain-of-function studies in the mouse embryonic nervous system.
Authors: Authors: Gaiano N, Kohtz JD, Turnbull DH, Fishell G.
Nat Neurosci
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BMPs: time to murder and create?
Authors: Authors: Fishell G.
Nat Neurosci
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Regionalization within the mammalian telencephalon is mediated by changes in responsiveness to Sonic Hedgehog.
Authors: Authors: Kohtz JD, Baker DP, Corte G, Fishell G.
Development
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Generation of a radial-like glial cell line.
Authors: Authors: Friedlander DR, Brittis PA, Sakurai T, Shif B, Wirchansky W, Fishell G, Grumet M.
J Neurobiol
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Telencephalic progenitors maintain anteroposterior identities cell autonomously.
Authors: Authors: Na E, McCarthy M, Neyt C, Lai E, Fishell G.
Curr Biol
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