GABAergic interneurons perform crucial roles in cerebral cortical development and function, but little is known about the molecular mechanisms that control interneuron fate determination. Most cortical interneurons originate in the medial ganglionic eminence (MGE) of the ventral forebrain, where recent evidence has begun to further define the origins of distinct subgroups of cortical interneurons (Xu...Anderson, 2004). The experiments described below are designed to examine how molecular signals specify interneurons within the MGE. To achieve this goal we will use a combination of in vivo and in vitro gain and loss of function studies focused on four proteins: 1) Sonic Hedgehog (Shh), a morphogen that promotes ventral neural tube development including the MGE, 2) NKX2.1, a transcription factor target of Shh signaling that is required for normal MGE development, 3) LHX6, a transcription factor that is, downstream of Nkx2.1 in the MGE and is expressed in interneurons migrating to the cerebral cortex, 4) ARX1, also expressed in migrating interneurons, and required for normal interneuron development. Since mutations inShh, Nkx2.1 and Arx1 have been linked to developmental forebrain abnormalities in humans, these studies lay the groundwork for identifying the """"""""molecular code"""""""" for interneuron specification that will enhance our understanding of and treatment approaches for a variety of neuropathologic conditions. In addition, these studies are highly synergistic with other aims of the PPG including;the molecular control of cortical and subcortical proliferation by cyclin D2 and Shh (Projects 1 and 3), the role of migratory subcortical interneurons in cortical proliferation (Project 3) and the histological, physiological and behavioral effects of altered interneuron output by the MGE (Projects 1 and 4). In sum, the overarching goal of this project is to link clinically relevant alterations in embryonic forebrain development with postnatal histological and functional phenotypes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Program Projects (P01)
Project #
5P01NS048120-05
Application #
8097465
Study Section
Special Emphasis Panel (ZNS1)
Project Start
Project End
Budget Start
2010-07-01
Budget End
2011-06-30
Support Year
5
Fiscal Year
2010
Total Cost
$216,830
Indirect Cost
Name
Weill Medical College of Cornell University
Department
Type
DUNS #
060217502
City
New York
State
NY
Country
United States
Zip Code
10065
Sultan, Khadeejah T; Shi, Song-Hai (2018) Generation of diverse cortical inhibitory interneurons. Wiley Interdiscip Rev Dev Biol 7:
Sudarov, Anamaria; Zhang, Xin-Jun; Braunstein, Leighton et al. (2018) Mature Hippocampal Neurons Require LIS1 for Synaptic Integrity: Implications for Cognition. Biol Psychiatry 83:518-529
Chohan, Muhammad O; Moore, Holly (2016) Interneuron Progenitor Transplantation to Treat CNS Dysfunction. Front Neural Circuits 10:64
Sultan, Khadeejah T; Han, Zhi; Zhang, Xin-Jun et al. (2016) Clonally Related GABAergic Interneurons Do Not Randomly Disperse but Frequently Form Local Clusters in the Forebrain. Neuron 92:31-44
Tan, Xin; Liu, Wenying Angela; Zhang, Xin-Jun et al. (2016) Vascular Influence on Ventral Telencephalic Progenitors and Neocortical Interneuron Production. Dev Cell 36:624-38
Marcucci, Florencia; Murcia-Belmonte, Veronica; Wang, Qing et al. (2016) The Ciliary Margin Zone of the Mammalian Retina Generates Retinal Ganglion Cells. Cell Rep 17:3153-3164
Petros, Timothy J; Bultje, Ronald S; Ross, M Elizabeth et al. (2015) Apical versus Basal Neurogenesis Directs Cortical Interneuron Subclass Fate. Cell Rep 13:1090-1095
Sultan, Khadeejah T; Shi, Wei; Shi, Song-Hai (2014) Clonal origins of neocortical interneurons. Curr Opin Neurobiol 26:125-31
Xu, Hua-Tai; Han, Zhi; Gao, Peng et al. (2014) Distinct lineage-dependent structural and functional organization of the hippocampus. Cell 157:1552-64
Mirzaa, Ghayda; Parry, David A; Fry, Andrew E et al. (2014) De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome. Nat Genet 46:510-515

Showing the most recent 10 out of 36 publications