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In‐depth characterization of the secretome of mouse CNS cell lines by LC‐MS/MS without prefractionation
Author(s) -
Woo Jongmin,
Han Dohyun,
Park Joonho,
Kim Sang Jeong,
Kim Youngsoo
Publication year - 2015
Publication title -
proteomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.26
H-Index - 167
eISSN - 1615-9861
pISSN - 1615-9853
DOI - 10.1002/pmic.201400623
Subject(s) - proteomics , secretory protein , biology , central nervous system , microglia , microbiology and biotechnology , cell culture , cell , brain cell , proteome , computational biology , neuroscience , bioinformatics , secretion , biochemistry , gene , immunology , genetics , inflammation
Microglia, astrocytes, and neurons, which have important functions in the central nervous system (CNS), communicate mutually to generate a signal through secreted proteins or small molecules, but many of which have not been identified. Because establishing a reference for the secreted proteins from CNS cells could be invaluable in examining cell-to-cell communication in the brain, we analyzed the secretome of three murine CNS cell lines without prefractionation by high-resolution mass spectrometry. In this study, 2795 proteins were identified from conditioned media of the three cell lines, and 2125 proteins were annotated as secreted proteins by bioinformatics analysis. Further, approximately 500 secreted proteins were quantifiable as differentially expressed proteins by label-free quantitation. As a result, our secretome references are useful datasets for the future study of neuronal diseases. All MS data have been deposited in the ProteomeXchange with identifier PXD001597 (http://proteomecentral.proteomexchange.org/dataset/PXD001597).