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dc.contributor.authorShepherd, Joanna
dc.contributor.authorHilderbrand, Scott A.
dc.contributor.authorWaterman, Peter
dc.contributor.authorHeinecke, Jay W.
dc.contributor.authorWeissleder, Ralph
dc.contributor.authorLibby, Peter
dc.date.accessioned2019-09-21T03:36:11Z
dc.date.issued2007
dc.identifier.citationShepherd, Joanna, Scott A. Hilderbrand, Peter Waterman, Jay W. Heinecke, Ralph Weissleder, and Peter Libby. 2007. “A Fluorescent Probe for the Detection of Myeloperoxidase Activity in Atherosclerosis-Associated Macrophages.” Chemistry & Biology 14 (11): 1221–31. https://doi.org/10.1016/j.chembiol.2007.10.005.
dc.identifier.issn1074-5521
dc.identifier.issn1879-1301
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:41384269*
dc.description.abstractThe myeloperoxidase (MPO)-derived oxidant hypochlorous acid (HOCI/OCI-) is implicated in the pathogenesis of atherosclerosis and other inflammatory states. We have synthesized an imaging probe, sulfonaphthoamino-phenyl fluorescein (SNAPF), that selectively reacts with HOCI. SNAPF detects HOCI produced by stimulated MPO-expressing cells cultured from human whole blood, as well as HOCI from bone marrow (BM)-derived macrophages isolated from transgenic mice that express human MPO. Two lines of evidence indicate that SNAPF permits the in vivo imaging of HOCI production. First, we used this approach to demonstrate HOCI production by neutrophils in experimental murine peritonitis. Second, we detected HOCI production by MPO expressing cells in human atherosclerotic arteries. Thus, fluorescence reflectance imaging by SNAPF may provide a valuable noninvasive molecular imaging tool for implicating HOCI and MPO in the damage of inflamed tissues.
dc.language.isoen_US
dc.publisherElsevier (Cell Press)
dash.licenseLAA
dc.titleA novel fluorescent probe for the detection of myeloperoxidase activity in atherosclerosis-associated macrophages
dc.typeJournal Article
dc.description.versionAccepted Manuscript
dc.relation.journalChemistry & Biology
dash.depositing.authorWeissleder, Ralph::ea07ce19f187d4fab47c56ee97fa5c5a::600
dc.date.available2019-09-21T03:36:11Z
dash.workflow.comments1Science Serial ID 23489
dc.identifier.doi10.1016/j.chembiol.2007.10.005
dash.source.volume14;11
dash.source.page1221


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