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The major cell classes of the brain differ in their developmental processes, metabolism, signaling, and function. To better understand the functions and interactions of the cell types that comprise these classes, we acutely purified representative populations of neurons, astrocytes, oligodendrocyte precursor cells, newly formed oligodendrocytes, myelinating oligodendrocytes, microglia, endothelial cells, and pericytes from mouse cerebral cortex. We generated a transcriptome database for these eight cell types by RNA sequencing and used a sensitive algorithm to detect alternative splicing events in each cell type. Bioinformatic analyses identified thousands of new cell type-enriched genes and splicing isoforms that will provide novel markers for cell identification, tools for genetic manipulation, and insights into the biology of the brain. For example, our data provide clues as to how neurons and astrocytes differ in their ability to dynamically regulate glycolytic flux and lactate generation attributable to unique splicing of PKM2, the gene encoding the glycolytic enzyme pyruvate kinase. This dataset will provide a powerful new resource for understanding the development and function of the brain. To ensure the widespread distribution of these datasets, we have created a user-friendly website (http: //web. stanford. edu/group/barresₗab/brainᵣnaseq. html) that provides a platform for analyzing and comparing transciption and alternative splicing profiles for various cell classes in the brain.
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Ye Zhang
Army Medical University
Kenian Chen
The University of Texas Southwestern Medical Center
Steven A. Sloan
Emory University
Journal of Neuroscience
Stanford University
University of California, San Francisco
The University of Melbourne
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Zhang et al. (Wed,) studied this question.
synapsesocial.com/papers/69d89c8c183921ebcaae2e7d — DOI: https://doi.org/10.1523/jneurosci.1860-14.2014