@article{3ac3d147eebe4900849f7b0775ad83c1,
title = "FACS-array profiling of striatal projection neuron subtypes in juvenile and adult mouse brains",
abstract = "A major challenge in systems neuroscience is to perform precise molecular genetic analyses of a single neuronal population in the context of the complex mammalian brain. Existing technologies for profiling cell type-specific gene expression are largely limited to immature or morphologically identifiable neurons. In this study, we developed a simple method using fluorescent activated cell sorting (FACS) to purify genetically labeled neurons from juvenile and adult mouse brains for gene expression profiling. We identify and verify a new set of differentially expressed genes in the striatonigral and striatopallidal neurons, two functionally and clinically important projection neuron subtypes in the basal ganglia. We further demonstrate that Ebf1 is a lineage-specific transcription factor essential to the differentiation of striatonigral neurons. Our study provides a general approach for profiling cell type-specific gene expression in the mature mammalian brain and identifies a set of genes critical to the function and dysfunction of the striatal projection neuron circuit.",
author = "Lobo, {Mary Kay} and Karsten, {Stanislav L.} and Michelle Gray and Geschwind, {Daniel H.} and Yang, {X. William}",
note = "Funding Information: We would like to thank N. Heintz (Rockefeller University) and the National Institute of Neurological Disorders and Stroke (NINDS) Gene Expression Nervous System Atlas (GENSAT) program for providing the BAC transgenic mice; R. Grosschedl (Max-Planck-Institute of Immunobiology, Freiburg, Germany) for the Ebf1 knockout mice; M.S. Levine for equipment use; C. Evans for the met-Enkephalin antibody; D. Anderson (California Institute of Technology) for advice on cell dissociation; and S.L. Zipursky, A. Silva, D.E. Krantz, Y.E. Sun, M.S. Levine and members of the Yang lab for discussions. We would like to thank the UCLA Jonsson Comprehensive Cancer Center and Center for AIDS Research Flow Cytometry Core Facility, and UCLA NINDS/ National Institute of Mental Health (NIMH) DNA Microarray Core Facility for their services. X.W.Y. is supported by Semel Institute for Neuroscience and Human Behaviors, NINDS (NS049501 and NS047391) and the Hereditary Disease Foundation, and by pilot grants from UCLA Hatos Center for Neuropharmacology (National Institute of Drug Abuse P50DA05010) and UCLA Brain Research Institute (supported by the Employees Charity Organization of Northrup Grumman). M.K.L. and M.G. are supported by UCLA Mental Retardation Research Center training grants (5T32HD007032 from National Institute of Child Health and Human Development). M.G. is also supported by UCLA Center for Neurobehavioral Genetics (5T32NS048004 from NINDS). D.H.G. is supported by NINDS/NIMH U24 NS43562. S.L.K. is supported by the French Foundation for Alzheimer{\textquoteright}s Research.",
year = "2006",
month = mar,
doi = "10.1038/nn1654",
language = "English",
volume = "9",
pages = "443--452",
journal = "Nature Neuroscience",
issn = "1097-6256",
publisher = "Nature Publishing Group",
number = "3",
}