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The Proteome of Mouse Brain Microvessel Membranes and Basal Lamina
Author(s) -
Hyun Bae Chun,
Michael M. Scott,
Sherry Niessen,
Heather Hoover,
Andrew Baird,
John R. Yates,
Bruce E. Torbett,
Brian P. Eliceiri
Publication year - 2011
Publication title -
journal of cerebral blood flow and metabolism
Language(s) - English
Resource type - Journals
eISSN - 1559-7016
pISSN - 0271-678X
DOI - 10.1038/jcbfm.2011.104
Subject(s) - tight junction , basal lamina , microbiology and biotechnology , microvessel , biology , proteome , transcriptome , parenchyma , blood–brain barrier , context (archaeology) , extracellular matrix , membrane protein , pericyte , endothelial stem cell , membrane , neuroscience , angiogenesis , anatomy , biochemistry , gene expression , in vitro , central nervous system , gene , ultrastructure , paleontology , botany , cancer research
The blood–brain barrier (BBB) is a multicellular vascular structure separating blood from the brain parenchyma that is composed of endothelial cells with tight intercellular junctions, surrounded by a basal lamina, astrocytes, and pericytes. Previous studies have generated detailed databases of the microvessel transcriptome; however, less information is available on the BBB at the protein level. In this study, we specifically focused on characterization of the membrane fraction of cells within the BBB to generate a more complete understanding of membrane transporters, tight junction proteins, and associated extracellular matrix proteins that are functional hallmarks of the BBB. We used Multidimensional Protein Identification Technology to identify a total of 1,143 proteins in mouse brain microvessels, of which 53% were determined to be membrane associated. Analyses of specific classes of BBB-associated proteins in the context of recent transcriptome reports provide a unique database to assess the relative contribution of genes at the level of both RNA and protein in the maintenance of normal BBB integrity.

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