期刊
JOURNAL OF PROTEOMICS
卷 103, 期 -, 页码 227-240出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.jprot.2014.04.008
关键词
LC MS; Label-free quantitation; Microvesicles; Exosomes; Hepatocytes; Liver
资金
- Fondo de Investigaciones Sanitarias (Institute of Health Carlos III) [06/0621, P809/00526, PI12/01064]
- Program Ramon y Cajal of Spanish Ministry (PRYC) [2007-00228]
- National Institute of Health [RO1 AT004896]
- Centro de Investigacion Biomedica en Red en el Area tematica de Enfermedades Hepaticas y Digestivas (CIBERehd)
Extracellular vesicles have created great interest as possible source of biomarkers for different biological processes and diseases. Although the biological function of these vesicles is not fully understood, it is clear that they participate in the removal of unnecessary cellular material and act as carriers of various macromolecules and signals between the cells. In this report, we analyzed the proteome of extracellular vesicles secreted by primary hepatocytes. We used one- and two-dimensional liquid chromatography combined with data-independent mass spectrometry. Employing label-free quantitative proteomics, we detected significant changes in vesicle protein expression levels in this in vitro model after exposure to well-known liver toxins (galactosamine and Escherichia coli-derived lipopolysaccharide). The results allowed us to identify candidate markers for liver injury. We validated a number of these markers in vivo, providing the basis for the development of novel methods to evaluate drug toxicity. This report strongly supports the application of proteomics in the study of extracellular vesicles released by well-controlled in vitro cellular systems. Analysis of such systems should help to identify specific markers for various biological processes and pathological conditions. Biological significance Identification of low invasive candidate marker for hepatotoxicity. Support to apply proteomics in the study of extracellular vesicles released by well-controlled in vitro cellular systems to identify low invasive markers for diseases. (C) 2014 Elsevier B.V. All rights reserved.
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