Cell type– and brain region–resolved mouse brain proteome
Author(s) -
Kirti Sharma,
Sebastian Schmitt,
Caroline G. Bergner,
Stefka Tyanova,
Nirmal Kannaiyan,
Natalia ManriqueHoyos,
Karina Kongi,
Ludovico CantutiCastelvetri,
UweKarsten Hanisch,
MariAnne Philips,
Moritz J. Rossner,
Matthias Mann,
Mikael Simons
Publication year - 2015
Publication title -
nature neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 13.403
H-Index - 422
eISSN - 1546-1726
pISSN - 1097-6256
DOI - 10.1038/nn.4160
Subject(s) - proteome , biology , transcriptome , proteomics , cell type , neuroscience , computational biology , cell , microglia , microbiology and biotechnology , bioinformatics , gene expression , genetics , gene , immunology , inflammation
Brain transcriptome and connectome maps are being generated, but an equivalent effort on the proteome is currently lacking. We performed high-resolution mass spectrometry-based proteomics for in-depth analysis of the mouse brain and its major brain regions and cell types. Comparisons of the 12,934 identified proteins in oligodendrocytes, astrocytes, microglia and cortical neurons with deep sequencing data of the transcriptome indicated deep coverage of the proteome. Cell type-specific proteins defined as tenfold more abundant than average expression represented about a tenth of the proteome, with an overrepresentation of cell surface proteins. To demonstrate the utility of our resource, we focused on this class of proteins and identified Lsamp, an adhesion molecule of the IgLON family, as a negative regulator of myelination. Our findings provide a framework for a system-level understanding of cell-type diversity in the CNS and serves as a rich resource for analyses of brain development and function.
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