| Literature DB >> 26523646 |
Kirti Sharma1, Sebastian Schmitt2,3, Caroline G Bergner2,3, Stefka Tyanova1, Nirmal Kannaiyan4, Natalia Manrique-Hoyos2,3, Karina Kongi5, Ludovico Cantuti2,3, Uwe-Karsten Hanisch6, Mari-Anne Philips5, Moritz J Rossner2,4, Matthias Mann1, Mikael Simons2,3.
Abstract
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.Entities:
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Year: 2015 PMID: 26523646 PMCID: PMC7116867 DOI: 10.1038/nn.4160
Source DB: PubMed Journal: Nat Neurosci ISSN: 1097-6256 Impact factor: 24.884