Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/137002
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dc.contributor.authorSerra, Aidaen_US
dc.contributor.authorGallart-Palau, Xavieren_US
dc.contributor.authorPark, Jung Eunen_US
dc.contributor.authorLim, Grace Gui Yinen_US
dc.contributor.authorLim, Kah Leongen_US
dc.contributor.authorHo, Hee Hwaen_US
dc.contributor.authorTam, James Pingkwanen_US
dc.contributor.authorSze, Siu Kwanen_US
dc.date.accessioned2020-02-11T08:11:24Z-
dc.date.available2020-02-11T08:11:24Z-
dc.date.issued2018-
dc.identifier.citationSerra, A., Gallart-Palau, X., Park, J. E., Lim, G. G. Y., Lim, K. L., Ho, H. H., . . . Sze, S. K. (2018). Vascular bed molecular profiling by differential systemic decellularization in vivo, Arteriosclerosis, Thrombosis, and Vascular Biology, 38, 10, 2396-2409. doi:10.1161/ATVBAHA.118.311552en_US
dc.identifier.issn1079-5642en_US
dc.identifier.urihttps://hdl.handle.net/10356/137002-
dc.description.abstractObjective- Vascular endothelial dysfunction is a key component of several major human diseases, but the molecular basis of this complex disorder has been difficult to determine in vivo. Previous attempts to identify key mediators of vascular endothelial dysfunction in experimental models have been limited by the lack of suitable methods for system-wide analyses of vascular bed biology. Here, we aimed to develop a novel method for investigating vascular endothelial dysfunction pathogenesis that enables system-wide analyses of molecular interactions between endothelial glycocalyx, endothelial cells, and smooth muscle cells in murine. Approach and Results- We developed a new technique using whole-body differential perfusion with increasing concentrations of detergent buffer to selectively solubilize distinct layers of vascular bed tissue in rodents. When combined with proteomics techniques, our novel approach of differential systemic decellularization in vivo enabled quantitative profiling of vascular beds throughout the body. Initial perfusion with phosphate buffer was used to obtain the endothelial glycocalyx, followed by subsequent extraction of endothelial cell components, and finally by smooth muscle cell constituents with increasing concentrations of detergent. Differential systemic decellularization in vivo has also been successfully applied to characterize molecular events in the vascular bed pathology of lipopolysaccharide-challenged mice. Conclusions- Together, these data indicate that differential systemic decellularization in vivo permits system-wide molecular characterization of vascular bed proteomes in rodent models and can be used to advance our current understanding of vascular endothelial dysfunction pathogenesis and progression in a wide range of disease settings.en_US
dc.description.sponsorshipMOE (Min. of Education, S’pore)en_US
dc.description.sponsorshipNMRC (Natl Medical Research Council, S’pore)en_US
dc.language.isoenen_US
dc.relation.ispartofArteriosclerosis, Thrombosis, and Vascular Biologyen_US
dc.rights© 2018 American Heart Association, Inc. All rights reserved. This paper was published in Arteriosclerosis, Thrombosis, and Vascular Biology and is made available with permission of American Heart Association, Inc.en_US
dc.subjectScience::Biological sciencesen_US
dc.titleVascular bed molecular profiling by differential systemic decellularization in vivoen_US
dc.typeJournal Articleen
dc.contributor.schoolSchool of Biological Sciencesen_US
dc.identifier.doi10.1161/ATVBAHA.118.311552-
dc.description.versionAccepted versionen_US
dc.identifier.pmid30354219-
dc.identifier.scopus2-s2.0-85055601498-
dc.identifier.issue10en_US
dc.identifier.volume38en_US
dc.identifier.spage2396en_US
dc.identifier.epage2409en_US
dc.subject.keywordsCapillary Bedsen_US
dc.subject.keywordsEndothelial Cellsen_US
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