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Detection of the halogenating activity of heme peroxidases in leukocytes by aminophenyl fluorescein.
Flemmig, J; Remmler, J; Zschaler, J; Arnhold, J.
Affiliation
  • Flemmig J; Institute for Medical Physics and Biophysics, University of Leipzig , Leipzig , Germany.
Free Radic Res ; 49(6): 768-76, 2015 Jun.
Article in En | MEDLINE | ID: mdl-25536418
The formation of hypochlorous and hypobromous acids by heme peroxidases is a key property of certain immune cells. These products are not only involved in defense against pathogenic microorganisms and in regulation of inflammatory processes, but contribute also to tissue damage in certain pathologies. After a short introduction about experimental approaches for the assessment of the halogenating activity in vitro and in cell suspensions, we are focusing on novel applications of fluorescent dye systems to detect the formation of hypochlorous acid (HOCl) in leukocytes. Special attention is directed to properties and applications of the non-fluorescent dye aminophenyl fluorescein that is converted by HOCl, HOBr, and other strong oxidants to fluorescein. This dye allows the detection of the halogenating activity in samples containing free myeloperoxidase and eosinophil peroxidase as well as in intact granulocytes using fluorescence spectroscopy and flow cytometry, respectively.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peroxidase / Eosinophil Peroxidase / Halogenation / Fluoresceins / Fluorescent Dyes / Leukocytes / Aniline Compounds Type of study: Diagnostic_studies Limits: Animals / Humans Language: En Journal: Free Radic Res Journal subject: BIOQUIMICA Year: 2015 Document type: Article Affiliation country: Germany Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peroxidase / Eosinophil Peroxidase / Halogenation / Fluoresceins / Fluorescent Dyes / Leukocytes / Aniline Compounds Type of study: Diagnostic_studies Limits: Animals / Humans Language: En Journal: Free Radic Res Journal subject: BIOQUIMICA Year: 2015 Document type: Article Affiliation country: Germany Country of publication: United kingdom